AU2005256164A1 - Neurologically-active compounds - Google Patents

Description

WO 2006/000043 PCT/AU2005/000928 Neurologically-Active Compounds Technical Field 5 This invention relates to neurologically-active compounds. In particular, the invention relates to compounds that are antagonists of GABAc receptors, pharmaceutical compositions comprising the compounds and a method of enhancing the cognitive activity of an animal using the compounds. 10 Background of the Invention y-Aminobutyric acid (GABA) is the main inhibitory neurotransmitter in the central nervous system and activates the three major sub-types of GABA receptors in the 15 central nervous system, the GABAA, GABAB and GABAC receptors. The pharmacology of GABAA and GABAB receptors has been extensively investigated. GABAc receptors are the most recently described sub-type of GABA receptors, and are therefore the least studied sub-type. 20 GABAA receptors are ligand gated C1~ ion channels which are inhibited by the alkaloid bicuculline (Johnston, 1996a). GABAA receptors are heterooligomeric made up of cc, p, y, 8 and 0 subunits. GABAB receptors are transmembrane receptors coupled to second membrane messenger systems and Ca+ and K* channels via G-proteins. These receptors are not blocked by bicuculline, but are activated by (-)-baclophen and 3 25 aminopropylphosphinic acid (CGP27492) and blocked by saclofen (Kerr and Ong,, 1995). GABAc receptors (sometimes called GABANANB or p receptors) were first proposed when a series of conformationally restricted GABA analogues, including cis-4 30 aminocrotonic acid (CACA), that had bicuculline insensitive depression actions on neuronal activity, showed no affinity for [ 3 H]baclofen binding sites in rat cerebellar membranes (Drew et al, 1984). GABAc receptors with similar pharmacology were first found in neurons in rat retina (Feigenspan et al, 1993) and white perch retina (Qian et al, 1993). 35 Three major sub-types of GABAc receptors are now known, namely p1, p 2 and p3 (Chebib and Johnston, 2000).

WO 2006/000043 PCT/AU2005/000928 -2 GABA is a flexible compound, due to its rotation about the C2-C3 and C3-C4 bonds. It can exist in a range of low energy conformations (Johnston et al, 1978). Analogues of GABA in which two of these conformations have been restricted by the introduction of 5 unsaturation in the form of a double bond at the C2-C3 position have been prepared. Two compounds that represent these restricted conformations are CACA and trans-4 aminocrotonic acid (TACA) (Johnston et al, 1975). CACA and TACA have fewer degrees of rotational freedom than GABA, and can only rotate about the C3-C4 bond (Johnston et al, 1978). CACA is a partially folded analogue of GABA. It has moderate 10 activity at GABAc receptors expressed in Xenopus oocytes, and although its agonist activity is weak, it is to date the most selective agonist at these receptors, having minimal activity on GABAA and GABAB receptors (Johnston, 1996b). TACA is an extended analogue of GABA. It has potent agonist activity at GABAc receptors expressed in Xenopus oocytes; however, it is not selective, as it is also a potent GABAA 15 receptor agonist (Johnston, 1996b). Woodward et al (1993) tested many GABA analogues on poly (A)+RNA from mammalian retina expressed in Xenopus oocytes to determine a pharmaceutical profile for GABAc receptors. From this study, it was found that phosphinic and 20 methylphosphinic acid analogues of GABA, which are known to be potent GABAB receptor agonists, were potent antagonists at GABAc receptors. Several straight chain phosphinic, methylphosphinic and phosphonic acid analogues of GABA were shown to be potent antagonists at GABAc receptors, including (3-aminopropyl)methylphosphinic acid (CGP35024, KB=0.8 pLM), 3-aminoporpylphosphinic acid (CGP27492, KB=0.8 25 ptM) and 3-aminopropylphosphonic acid (3-APA, KB=1.8 pLM) (Woodward et al, 1993). These agents are not selective for GABAc receptors, as CGP35024 and CGP27492 are also very potent GABAB receptor agonists, while 3-APA is a GABAB receptor agonist. One of the most potent and selective GABAc receptor antagonists known is (1,2,5,6 30 tetrahydropyridine-4-yl)methylphosphinic acid (TPMPA, KB=2. 1p [M) (Murata et al, 1996; Ragozzinno et al, 1996). TPMPA produces 50% inhibition of GABAc receptor activation at 2.1 pM. Chebib et al, 1997 demonstrated that TPMPA, the phosphinic and methyl phosphinic 35 acid analogues of CACA and the closely related analogue TACA, and 3-aminopropyl-n butyl-phosphinic acid (CGP36742), an orally active GABAB receptor antagonist, are GABAc receptor antagonists.

WO 2006/000043 PCT/AU2005/000928 -3 It has been shown that GABAc receptor antagonists have therapeutic application. Froestl et al., 1995 investigated a series of GABAB receptor antagonists in various 5 memory and learning tests in rats and mice. Only one compound in this series, 3 aminopropyl-n-butyl-phosphinic acid (CGP36742), reversed age related deficits of old rats. The cognition-enhancing effects of this compound were confirmed in learning experiments in monkeys (Froestl et al., 1995). 10 The cognition-enhancing effects of CGP36742 is not satisfactorily explained by its GABAB antagonist properties, since much more potent GABAB antagonists have been described that do not have these effects. Some of the present inventors have previously shown that CGP36742 has similar potency as a GABAc antagonist to its potency as a GABAB antagonist (50% inhibition of receptor activation being found at 38 ptM and 62 15 piM against GABAB and GABAc receptors respectively) (Chebib et al., 1997). None of the other potent GABAB antagonists used in Froestl et al., 1995 showed activity against GABAc receptors. These findings indicate a role for GABAc receptor antagonism in the cognition-enhancing properties of CGP36742 reported in Froestl et al., 1995. 20 WO 98/58939 describes a method of enhancing the cognitive activity of an animal in need of such treatment, comprising the step of administering an effective amount of a compound which has GABAc receptor antagonist activity to said animal. That document also describes a method of stimulating memory capacity, comprising the step of administering an effective amount of a compound which has GABAc receptor 25 antagonist activity to an animal in need of such treatment. The document also describes novel compounds having GABAc receptor antagonist activity of the general formula I and general formula II as defined in that document. Most of the GABAc receptor antagonists described in the prior art, such as CGP36742, 30 are non-selective, that is, they also have significant activity at the GABAA or GABAB receptors. The use of such compounds as GABAc receptor antagonists may have undesirable side-effects via their action at the GABAA and/or GABAB receptors. WO 03/045897 describes compounds of formula I and formula II as defined in that 35 document. The compounds of formula I and formula II as defined in that document are selective GABAc receptor antagonists.

WO 2006/000043 PCT/AU2005/000928 -4 It would be desirable to identify other selective antagonists of the GABAc receptors. Selective antagonists of the GABAc receptors are needed to provide therapeutic agents with a lower risk of unwanted side-effects due to actions at the GABAA and/or GABAB receptors than the prior art non-selective GABAc receptor antagonists. 5 Summary of the Invention The inventors have found a class of compounds which are surprisingly selective GABAC receptor antagonists. 10 In a first aspect, the present invention provides a compound of the formula I: R -,// 15 /P NH2 H O (I) 20 wherein R is methyl, ethyl, propyl, isopropyl, butyl, pentyl, neo-pentyl or cyclohexyl, or a salt or solvate thereof. The compounds of formula I can exist in two stereoisomers. The present invention 25 encompasses racemic mixtures of the stereoisomers of the compounds of formula I, as well as the individual stereoisomers. The two stereoisomers of the compounds of the formula I are as follows: 30 0 R -,/

NH

2

HO

WO 2006/000043 PCT/AU2005/000928 -5 0 R \NH2 HO Each of these isomers is encompassed by the present invention. 5 The compounds of formula I are GABA analogues that are conformationally restricted by incorporating the backbone of GABA into a cyclopentene ring. This conformational restriction makes it difficult for the compounds to act at either GABAA or GABAB receptors, making these compounds selective GABAc antagonists. 10 In a second aspect, the present invention provides a method of selectively antagonising GABAc receptors compared with GABAB or GABAA receptors, comprising the step of exposing the receptors to an effective amount of a compound of formula I as defined above or a pharmaceutically acceptable salt or solvate thereof. 15 In a third aspect, the present invention provides a method of enhancing the cognitive activity of an animal, comprising the step of administering to the animal an effective amount of a compound of formula I as defined above or a pharmaceutically acceptable salt or solvate thereof. 20 In a fourth aspect, the present invention provides a method of stimulating memory capacity in an animal, comprising the step of administering to the animal an effective amount of a compound of formula I as defined above or a pharmaceutically acceptable salt or solvate thereof. 25 The methods of the present invention are suitable for the treatment of a variety of cognitive deficit conditions, dementias and memory impairment conditions, including but not limited to those associated with Alzheimer's disease, AIDS and schizophrenia. 30 While the invention is not restricted to the treatment of any particular animal species, in general, the animal is a human. In another aspect, the present invention provides the use of a compound of formula I as WO 2006/000043 PCT/AU2005/000928 -6 defined above or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for selectively antagonising GABAc receptors compared with GABAB or GABAA receptors. 5 In another aspect, the present invention provides the use of a compound of formula I as defined above or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for enhancing the cognitive activity of an animal. In another aspect, the present invention provides the use of a compound of formula I as 10 defined above or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for stimulating memory capacity in an animal. In another aspect, the present invention provides a pharmaceutical composition comprising a compound of formula I as defined above or a pharmaceutically acceptable 15 salt or solvate thereof, and a pharmaceutically acceptable carrier. Detailed Description of Preferred Embodiments The compounds of formula I are potent and selective antagonists of the GABAc 20 receptors, that is, they are potent antagonists of the GABAc receptors and are more active at one or more of the GABAC receptor sub-types than at the GABAA and GABAB receptors. In some embodiments of the present invention, R is selected from the group consisting 25 of methyl, ethyl, propyl, isopropyl and butyl. In one embodiment of the present invention, R is methyl. In another embodiment, R is ethyl. In other embodiments, R is propyl or isopropyl. In a preferred embodiment of the present invention, R is butyl. The compound of 30 formula I where R is butyl, has a butyl substituted phosphinic acid group in the 1-position of the cyclopentene ring corresponding to the carboxylic acid functionality of GABA. This substituent enhances the lipid solubility of the compound and thus increases the ability of the compound to cross the blood brain barrier. 35 As will be apparent to a person skilled in the art, various salts of the compounds of formula I can be prepared. Such salts include, for example, metal salts, ammonium salts, salts with an organic base, salts with an inorganic acid, and salts with an organic WO 2006/000043 PCT/AU2005/000928 -7 acid. Examples of metal salts include alkali metal salts, such as a sodium salt or a potassium salt. Examples of salts with an inorganic acid include salts with acids such as hydrochloric acid or hydrobromic acid. Examples of salts with organic acids include salts with acetic acid, trifluoroacetic acid, citric acid or formic acid. 5 The salts of the compounds of formula I are preferably pharmaceutically acceptable, but it will be appreciated that non-pharmaceutically acceptable salts also fall within the scope of the first aspect of the present invention. Non-pharmaceutically acceptable salts are useful as intermediates in the preparation of pharmaceutically acceptable salts. 10 Examples of pharmaceutically acceptable salts include salts of pharmaceutically acceptable cations such as sodium, potassium, lithium, calcium, magnesium, ammonium and alkylammonium; acid addition salts of pharmaceutically acceptable inorganic acids such as hydrochloric, orthophosphoric, sulphuric, phosphoric, nitric, carbonic, boric, sulfamic and hydrobromic acids; or salts of pharmaceutically 15 acceptable organic acids such as acetic, propionic, butyric, tartaric, maleic, hydroxymaleic, fumaric, citric, lactic, mucic, gluconic, benzoic, succinic, oxalic, phenylacetic, methanesulphonic, trihalomethanesulphonic, toluenesulphonic, benzenesulphonic, salicylic, sulphanilic, aspartic, glutamic, edetic, stearic, palmitic, oleic, lauric, pantothenic, tannic, ascorbic and valeric acids. 20 In addition, some of the compounds of the present invention may form solvates with water or common organic solvents. Such solvates are encompassed within the scope of the present invention. 25 The compounds of formula I as defined above or a pharmaceutically acceptable salt or solvate thereof, may be administered to an animal at any suitable dose and by any suitable route. The compounds may, for example, be administered orally or parenterally in dosage unit formulations containing conventional pharmaceutically acceptable carriers. The term "parenteral" as used herein includes subcutaneous 30 injections, aerosol, intravenous, intramuscular, intrathecal, intracranial injection or infusion techniques. Oral administration is preferred because of its greater convenience and acceptability. The pharmaceutical compositions of the present invention comprise at least one 35 compound of formula I or a pharmaceutically acceptable salt or solvate thereof, together with one or more pharmaceutically acceptable carriers and optionally other therapeutic agents. Each carrier is "pharmaceutically acceptable" in the sense of being compatible WO 2006/000043 PCT/AU2005/000928 -8 with the other ingredients of the composition and not causing any substantially adverse reaction in the animal to which the composition is administered. The compositions may conveniently be presented in unit dosage form and may be prepared by methods well known in the art of pharmacy. 5 Suitable pharmaceutical compositions for administration by any desired route may be prepared by standard methods using pharmaceutically acceptable carriers known in the art, for example by reference to well known texts such as Remington: The Science and Practice of Pharmacy, 2000 ( 2 0th Edition), AR Gennaro (Ed), Lippincott Williams & 10 Wilkins, Philadelphia, PA 19106-3621, USA or Australian Prescription Products Guide, 2000 ( 2 9 th Edition), J Thomas (Ed), Australian Pharmaceutical Publishing Company Limited, Victoria, Australia. Such methods include the step of bringing into association the active ingredient with the 15 carrier which constitutes one or more accessory ingredients. In general, the compositions are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers or both, and then if necessary shaping the product. 20 The pharmaceutical compositions of the present invention may be formulated for oral administration as tablets, aqueous or oily suspensions, lozenges, troches, powders, granules, emulsions, capsules, syrups or elixirs. Compositions formulated for oral administration may contain one or more agents selected from the group of sweetening agents, flavouring agents, colouring agents and preserving agents in order to produce a 25 pharmaceutically elegant and palatable preparation. When the pharmaceutical composition of the present invention is in the form of a tablet suitable for oral administration, the tablet contains the compound of formula I as defined above or a pharmaceutically acceptable salt or solvate thereof in admixture with 30 one or more pharmaceutically acceptable carriers. These pharmaceutically acceptable carriers may include, for example, (1) inert diluents, such as calcium carbonate, lactose, calcium phosphate or sodium phosphate; (2) granulating and disintegrating agents, such as corn starch or alginic acid; (3) binding agents, such as starch, gelatine or acacia; and (4) lubricating agents, such as magnesium stearate, stearic acid or talc. The tablets may 35 be uncoated or coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monostearate or glycol distearate may WO 2006/000043 PCT/AU2005/000928 -9 be employed. Pharmaceutical compositions for parenteral administration are typically in the form of sterile aqueous or non-aqueous solutions, suspensions, or emulsions. Suitable 5 pharmaceutically acceptable carriers for such compositions include non-aqueous carriers such as propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate, and aqueous carriers such as water and alcoholic/aqueous solutions, including saline and buffered media. The pharmaceutical composition may also include-preservatives and other additives such as, 10 for example, anti-microbials, anti-oxidants, chelating agents, and the like. The present invention provides a method of enhancing the cognitive activity of an animal, the method comprising the step of administering to the animal an effective amount of a compound of formula I as defined above or a pharmaceutically acceptable 15 salt or solvate thereof. The present invention also provides a method of stimulating memory capacity in an animal, the method comprising the step of administering to the animal an effective amount of a compound of formula I as defined above or a pharmaceutically acceptable salt or solvate thereof. As used herein, the term "effective amount" refers to an amount effective to yield the desired therapeutic response. 20 Typically the animal is a human. However, in some embodiments, the animal is a non human animal, for example a companion animal such as a dog or cat, or a domestic animal such as a horse, pony, donkey, mule, llama, alpaca, pig, cattle or sheep, or a zoo animal such as a non-human primate, a felid, a canid, a bovid or an ungulate. 25 The effective amount of the compound will depend on the nature of the condition to be treated, the age, weight and underlying state of health of the individual to be treated, the duration of treatment, the nature of concurrent therapy (if any) and the specific formulation employed. The dosage administered will be at the discretion of the 30 attending physician or veterinarian. The effective amount may readily be determined by those skilled in the art by trial and error experimentation, using methods which are well known in the art.

WO 2006/000043 PCT/AU2005/000928 - 10 Examples The invention is described below in detail by reference to the following non-limiting 5 examples. Example 1 - Synthesis Compounds of formula I in which R is methyl, ethyl, isopropyl or butyl (compounds (15), (16), (17) and (18) respectively) were prepared as outlined in the reaction Scheme 10 1 described below. A similar process can be used to prepare the compound of formula I in which R is propyl. In addition to the compounds of formula I (compounds (15), (16), (17) and (18)) a similar compound in which R is benzyl was also prepared (compound (19)). 15 In the following Schemes, Me = methyl, Et = ethyl, iPr = isopropyl, Bu = butyl and Bz = benzyl. 0 Na2CO3, MeOH o 0 Hydroquinone, Acetic Acid O OH Br2 0 Na2HPO4 (1) (2) O DMAP, Et3N, TDMSCI -OEtTfO L-selectride, Et3N 0 H\OTBDMS : OTBDMS R N-phenyltriflimide Pd(O)(PPh3)4, DABCO (4) (3) O 1) HN3, PPh3, DIAD R 0 // TBAF, THE R /O 2) 6M HCL, reflux R / P -P. P EtO OTBDMS EtO OH HO

NH

2 R = Me (5) R = Me (10) R = Me (15) R = Et (6) R = Et (11) R = Et (16) R = iPr (7) R = iPr (12) R = iPr (17) R = Bu (8) R = Bu (13) R = Bu (18) R = Bz (9) R = Bz (14) R = Bz (19) 20 Scheme 1: Synthesis of racemic 4-aminocyclopent-1-enyl phosphinic acids WO 2006/000043 PCT/AU2005/000928 - 11 OH 0 1. MeOH, p-TsOH, R OH dimethoxypropane 0 NaI, Acetone 0 HO 2. LiAH 4 , THF \' R O HO 3. Pyridine, TsC1 (20) R=CO 2 Me (23) (21) R=CH 2 OH (22) R=CH 2 OTs 0 1 BuLi, THF S S0 HO Amberlyst resin 0 Amberlyst resin 4 (acid form) HO (acid form) O HO'' O : HO"\ Me : Ox SMe (26) (25) (24) CSA, benzene HO* O O (27) Scheme 2: Synthesis of (-)-(S)-4-hydroxycyclopent-2-en-1-one OH 0 1. MeOH, p-TsOH, R -'IOH dimethoxypropane Oh. NaI, Acetone Oi,, H01- 2. LiAIH4, THF o - > K.I HO 3. Pyridine, TsC1 (28) R=CO 2 Me (31) (29) R=CH 2 OH (30) R=CH 2 OTs BuLi, THF S S N I Amberlyst resin 0 Amberlyst resin 0 H (acid form) HO, Me (acid form) O Me HO HO SMe XOwASMe (34) (33) (32) CSA, benzene HO/,O (35) 5 Scheme 3: Synthesis of (+)-(R)-4-hydroxycyclopent-2-en-1-one WO 2006/000043 PCT/AU2005/000928 - 12 The synthesis of (-)-(S)-hydroxycyclopent-2-en-1-one from L-tartaric acid would allow a person skilled in the art to synthesise optically active 4-aminocyclopent-1-enyl phosphinic acids using the methods shown in Scheme 1. Similarly, the synthesis of 5 (+)-(R)-hydroxycyclopent-2-en-1-one from D-tartaric acid would allow a person skilled in the art to synthesise optically active 4-aminocyclopent- 1 -enyl phosphinic acids using the methods shown in Scheme 1. All reagents used in the following Examples were of reagent grade or higher. 10 Tetrahydrofuran (THF) was freshly distilled from sodium benzophenone ketyl and all other solvents were distilled prior to use. 1 H and 13 C NMR were recorded on a Varian 300M instrument in the indicated solvents. All coupling constants (J values) are given in hertz. Low resolution mass spectra was recorded using either chemical ionization (LRCIMS) or electron impact (LREIMS). High resolution mass spectra was recorded 15 using electron impact only (HREIMS). Optical rotations were measured using a polar polarimeter and a 1dm cell. The following examples detail the reactions shown in Scheme 2. 20 Dimethyl 2,3-O-isopropylidene-L-tartarate (20) A solution of L-tartaric acid (80g, 533mol), p-toluenesulfonic acid (0.32g, 1.86mmol) and 2,2-dimethoxypropane (127g, 1.2mol) was refluxed gently with stirring for 1.5 hours. Cyclohexane and further 2,2-diemthoxypropane (63.7ml, 0.63mol) was added and azeotropes slowly removed form the head of a vigreaux column. After 25 approximately three days the solution was allowed to cool to room temperature and anhydrous potassium carbonate added to neutralize the catalyst. The solution was then filtered and the solvent removed in-vacuo. The crude product was then distilled at high vacuum to give dimethyl 2,3-0-isopropylidene-L-tartarate (90g, 412mmol 78%) as a yellow oil. 1 H NMR (CDCl 3 ): 8 4.85 (s, 2H), 3.86 (s, 6H), 1.53 (s, 6H); "C NMR 30 (CDCl 3 ): 5 172.16, 114.13, 72.25, 53.40, 26.55; LRCIMS: 218.9 (M+1). 2,3-0-Isopropylidene-L-threiotol (21) Lithium aluminium hydride (10g, 267mmol) in anhydrous THF (120ml) was refluxed under nitrogen for thirty minutes with stirring. A solution of dimethyl 2,3-0- WO 2006/000043 PCT/AU2005/000928 - 13 isopropylidene-L-tartarate (20) (53g, 243mmol) in anhydrous THF (200ml) was added dropwise with stirring. The heat of addition resulted in a gentle reflux. The solution was then refluxed for an additional 3 hours, after which the solution was cooled to 0*C. Water (8.4ml), sodium hydroxide (4M, 8.4ml) and water (32ml) were consecutively 5 added to the solution. The resulting precipitate was removed from the solution by filtration and extracted with diethyl ether (soxhlet). The combined extracts were dried and evaporated at reduced pressure to give 2,3-0-isopropylidene-L-threiotol (35g, 216mmol, 89%). 1H NMR (CDCl 3 ): 8 3.98 (in, 2H), 3.77 (in, 4H), 3.64 (s, 2H), 1.45 (s, 6H); 1 3 C NMR (CDCl 3 ): 8 109.53, 78.24, 62.25, 27.28; LREIMS: 162.1 (M). The crude 10 product can be used in the next step. 1,4-Ditosyl-2,3-0-isopropylidene-L-threitol (22) A solution of 2,3-0-isopropylidene-L-threiotol (21) (35g, 216mmol) in dry pyridine (500ml) was cooled to -1 0*C. Finely powdered p-tosylchloride (86g, 453mmol) was 15 added in one portion and the solution stirred until homogenous. The solution was then held at 0 0 C overnight without stirring. The product was then crystallized from the mixture by the slow addition of water at 0 0 C. Once visible crystals had begun to form, water was added more rapidly until 500mls of water had been added over three hours at 0*C. Crystallization was then allowed to continue for an additional 1.5 hours at which 20 stage the product was isolated by filtration and washed on the frit with water. The product was then re-crystallized from ethanol to give 1,4-ditosyl-2,3-0-isopropylidene L-threitol (65g, 138mmol, 68%) as colourless crystals. 'H NMR (CDC1 3 ): 8 7.82 (d, J=8.2 , 2H), 7.40 (d, J=8.1 , 2H), 4.13 (m, 4H), 4.04 (in, 2H), 2.48 (s, 6H), 1.33 (s, 6); 1 3 C NMR (CDCl 3 ): 6 148.48, 132.70, 130.24, 128.26, 111.09, 75.32, 68.66, 26.99, 25 21.94; LRCIMS: 470.9 (M+1). 1,4-Dideoxy-1,4-diiodo-2,3-O-isopropylidene-L-threitol (23) To a solution of 1,4-ditosyl-2,3-O-isopropylidene-L-tbreitol (22) (65g, 138mmol) in dry acetone (800ml) was added sodium iodide (85g, 553mmol) and the mixture refluxed 30 overnight. The solution was then cooled to room temperature, filtered and the filtrate evaporated at reduced pressure. The residue was then dissolved in ethyl acetate (100ml), filtered, washed with water, sodium thiosulphate (5%), brine and then evaporated at reduced pressure. The crude product was then purified via flash chromatography on WO 2006/000043 PCT/AU2005/000928 - 14 silica gel (hexane 5% ethylacetate) to give 1,4-dideoxy-1,4-diiodo-2,3-0 isopropylidene-L-threitol (40.5g, 105mmol, 75.8%) as a yellow oil. 1H NMR (CDCl 3 ): 8 3.89 (in, 2H), 3.40 (in, 4H), 1.50 (s, 6); "C NMR (CDCl 3 ): 8 110.38, 80.84, 27.94, 6.94; LRCIMS: 382.6 (M+1). 5 (3S,4S)-3,4-O-Isopropylidene-threitolcyclopentanonedimethyldithioketal-S-oxide (24) To a solution of methyl methylsulfinyl sulfide (5g, 40mmol) in anhydrous THF (150ml) at -70'C under nitrogen was added butyl lithium (1.6M solution in hexane, 20ml), 10 dropwise over 15 minutes. The solution was stirred at -70*C for one hour before being allowed to warm slowly to room temperature and stirred for an additional one hour. The solution was then re-cooled to -70'C and 1,4-dideoxy-1,4-diiodo-2,3-0-isopropylidene L-threitol (23) was added dropwise over 20 minutes. The solution was then allowed to warm slowly to room temperature, heated to 25'C and stirred for an additional three 15 days under nitrogen. Saturated ammonium chloride (100ml) containing triethylamine (1ml) was then added with stirring. The aqueous phase was then separated and extracted with dichloromethane (2x50ml). The combined organic extracts were evaporated at reduced pressure and purified via flash chromatography on a silica gel column that was pre-treated with hexane containing 1% triethylamine and eluted with ethyl acetate 20 containing 20% acetone and 1% triethylamine to give (3S,4S)-3,4-0-isopropylidene threitolcyclopentanonedimethyldithioketal S-oxide (2.7g, 1 1mmol, 74%) as a colourless oil that crystallized upon standing. 1H NMR (CD 3 0D, major isomer): 5 4.17 (in, 1H), 2.74 (s, 3H), 2.72 (dd, 2H, J=6.7, J=12.9), 2.34 (s, 3H), 1.85 (dd, 2H, J=5.9, J=11.9), 1.50 (s, 6); 1H NMR (CD 3 0D, minor isomer): 5 3.90 (in, 1H), 2.68 (s, 3H), 2.54 (dd, 25 2H, J=6.9, J=12.4), 2.26 (s, 3H), 2.11 (dd, 2H, J=6.1, J=12.0), 1.53 (s, 6H); "C NMR

(CD

3 0D): 8 120.61, 81.49, 72.16, 34.25, 31.67, 26.23, 12.31. Instability prevented MS analysis. (3S,4S)-3,4-Dihydroxy-threitoleyclopentanonedimethyldithioketal-S-oxide (25) 30 To a solution of (3S,4S)-3,4-0-isopropylidene threitolcyclopentanonedimethyldithioketal-S-oxide (24) (1.9g) in methanol (20ml) and water (1ml) was added amberlyst resin (acid form, 0.3g). The solution was stirred for 15 minutes at room temperature and monitored by TLC. Upon consumption of the starting WO 2006/000043 PCT/AU2005/000928 - 15 material, the solution was filtered to remove the resin and neutralized with sodium bicarbonate. The solution was then filtered through florisil eluted with dichloromethane containing 10% methanol. The solvent was then removed at reduced pressure and the residue purified via flash chromatography on silica gel eluted with dichloromethane 5 containing 10% methanol to give (3S,4S)-3,4-dihydroxy threitolcyclopentanonedimethyldithioketal-S-oxide (1.L g, 69%) as a colourless oil. Minor Isomer 1 H NMR (CD 3 0D) 6 4.28 (in, 1H), 4.03 (in, 1), 2.78 (dd, 1, J=7.1, J=15.1), 2.70 (s, 3H), 2.59 (dd, 1H, J=7.7, J=14.6), 2.27 (s, 3H), 2.14 (dd, 1H, J=8.5, J=15.8), 1.75 (dd, 1H, J=5.8, J=13.5); 13 C NMR (CD 3 0D) 5 76.32, 73.91, 69.88, 43.92, 10 41.03, 20.97, 12.23 Major Isomer 1 H NMR (CD 3 0D) 6 4.15 (in, 1H), 3.93 (dd, 1H, J=6.3, J=8.3), 2.67 (s, 3H), 2.50 (dd, 1H, J=6.2, J=13.3), 2.34 (dd, 1H, J=4.3, J=11.1), 2.24 (s, 3H), 2.07 (dd, 1H, J=6.4, J=13.8), 1.96 (dd, 1H, J=6.7, J=13.9); "C NMR (CD 3 0D) 6 76.32, 73.91, 69.88, 43.92, 41.03, 20.97, 12.23. Instability prevented MS analysis. 15 (3S,4S)-3,4-Dihydroxycyclopentanone (26) To a solution of (3S,4S)-3,4-dihydroxy-threitolcyclopentanonedimethyldithioketal-S oxide (25) (1.1g) in methanol (10ml) and water (0.5ml) was added amberlyst resin (acid form, 2g). The solution was stirred for 3 hours at room temperature. Upon consumption 20 of the starting material, the solution was filtered to remove the resin and neutralized with sodium bicarbonate. The solution was then filtered through florisil eluted with dichloromethane containing 10% methanol. The solvent was then removed at reduced pressure, the residue redissolved in benzene (20ml) and dried in-vacuo to remove all water. The residue was then purified via flash chromatography on silica gel eluted with 25 dichloromethane containing 10% methanol to give (3S,4S)-3,4 dihydroxycyclopentanone (0.4g, 3mmol, 66%) as a colourless oil. 1H NMR (d 6 acetone): 6 4.42 (d, 2H, J=2.8), 4.33 (in, 211), 2.55 (dd, 2H, J=4.8, J=17.2), 2.05 (d, 2H, J=18.0); 1 3 C NMR (d 6 -acetone): 6 205.76, 74.21, 44.19; LRCIMS: 116.9 (M+1). 30 (-)-(S)-4-Hydroxycyclopent-2-en-1-one (27) A solution of (3S,4S)-3,4-dihydroxycyclopentanone (26) (0.4g, 3.4nmol) and a catalytic quantity of dl-10-camphorsulfonic acid (CSA) (10mg, 0.043mmol) in benzene (70 ml) was heated to reflux. Water was removed from the solution using a dean stark WO 2006/000043 PCT/AU2005/000928 - 16 apparatus. After approximately three hours the solution was concentrated to approximately 40 ml by removing solvent from the dean stark apparatus. The solution was then refluxed for a further 4 hours before having the solvent removed in-vacuo and purified via flash chromatography on silica gel eluted with dichloromethane containing 5 10% methanol to give (-)-(S)-4-hydroxycyclopent-2-en-1-one (0.17g, 1.7mmol, 53%) as a yellow oil. 'H NMR (CDCl 3 ):7.61 (dd, 1H, J=2.3, J=5.7), 6.25 (dd, 1H, J=1.3, J=5.7), 5.07 (m, 1H), 2.80 (dd, 1H, J=6.1, J=18.5), 2.30 (dd, 1H, J=2.2, J=18.5); 3 C-NMR (CDCl 3 ):S 207.8, 164.4, 134.5, 70.0, 44.1; [a]D = -89.7 (c=1.2) ee > 99%; LRCIMS: 99.0 (M+1). 10 As shown in Scheme 3, (+)-(R)-4-hydroxycyclopent-2-en-1-one (35) may be synthesized using D-tartaric acid as the starting material and source of chirality in a similar manner to that for (-)-(S)-4-hydroxycyclopent-2-en-1-one, as described above. The characteristics of each of the compounds shown in Scheme 3 (compounds (28) to 15 (35)) are detailed below. Dimethyl 2,3-0-isopropylidene-D-tartarate (28) (99%); 'H NMR (CDCl 3 ): 8 4.81 (s, 2H), 3.83 (s, 6H), 1.50 (s, 6); "C NMR (CDCl 3 ):8 170.28, 114.08, 77.21, 53.03, 26.53; GCCIMS: single peak @ 5.71 minutes m/z: 218.9 20 (M+1). 2,3-O-Isopropylidene-D-threiotol (29) (89%); 'H NMR (CDCl 3 ): 8 4.05 (m, 2H), 3.80 (m, 4H), 1.47 (s, 6H); 13 C NMR (CDCl 3 ):S 109.53, 78.14, 62.03, 27.29; LREIMS: 162.9 (M). 25 1,4-Ditosyl-2,3-O-isopropylidene-D-threitol (30) (93%); 'H NMR (CDCl 3 ): 8 7.82 (d, 2H, J=8.4), 7.40 (d, 2H, J=8.1), 4.13 (m, 4H), 4.05 (m, 2H), 2.49 (s, 6H), 1.33 (s, 6H); 1 3 C NMR (CDCl 3 ): 6 145.50, 132.70, 130.24, 128.26, 111.09, 75.30, 68.66, 26.98, 21.93; LRCIMS: 470.9 (M+1). 30 1,4-Dideoxy-1,4-diiodo-2,3-0-isopropylidene-D-threitol (31) (99%); 'H NMR (CDCl 3 ): 6 3.88 (m, 2H), 3.40 (m, 4H), 1.50 (s, 6H); 1 3 C NNR (CDCl 3 ):S 110.37, 80.51, 27.95, 6.59; GCCIMS: single peak @ 7.83 minutes m/z: 382.5 (M+1).

WO 2006/000043 PCT/AU2005/000928 - 17 (3R,4R)-3,4-O-Isopropylidene-threitolcyclopentanonedimethyldithioketal-S-oxide (32) (70%); 'H NMR (CD 3 OD, major isomer): 6 4.17 (m, 1H), 2.74 (s, 3H), 2.72 (dd, 2H, 5 J=6.7, J=12.9), 2.34 (s, 3H), 1.85 (dd, 2H, J=5.9, J=11.9), 1.50 (s, 6H); 'H NMR

(CD

3 0D, minor isomer): 6 3.90 (m, 1H), 2.68 (s, 3H), 2.54 (dd, 2H, J=6.9, J=12.4), 2.26 (s, 3H), 2.11 (dd, 2H, J=6.1, J=12.0), 1.53 (s, 6H); 1 3 C NMR (CD 3 0D): 6 120.61, 81.49, 72.16, 34.25, 31.67, 26.23, 12.31. 10 (3R,4R)-3,4-Dihydroxy-threitolcyclopentanonedimethyldithioketal-S-oxide (33) (90%); 1H NMR (minor isomer, CD 3 0D): 6 4.28 (m, 1H), 4.03 (m, 1H), 2.78 (dd, 1H, J=7.1, J=15.1), 2.70 (s, 3H), 2.59 (dd, 1H, J=7.7, J=14.6), 2.27 (s, 3H), 2.14 (dd, IH, J=8.5, J=15.8), 1.75 (dd, 1H, J=5.8, J=13.5); 1 3 C NMR (CD 3 0D) 6 76.32, 73.91, 69.88, 43.92, 41.03, 20.97, 12.23. 15 1H NMR (major isomer, CD 3 0D) 6 4.15 (m, 1H), 3.93 (dd, 1H, J=6.3, J=8.3), 2.67 (s, 3H), 2.50 (dd, 1H, J=6.2, J=13.3), 2.34 (dd, 1H, J=4.3, J=11.1), 2.24 (s, 3H), 2.07 (dd, 1H, J=6.4, J=13.8), 1.96 (dd, 1H, J=6.7, J=13.9); 1 3 C NMR (CD 3 0D) 8 76.32, 73.91, 69.88, 43.92, 41.03, 20.97, 12.23. 20 (3R,4R)-3,4-Dihydroxycyclopentanone (34) (75%); 'H NMR (CD 3 0D): 6 4.28 (dt, 2H, J=1.6, J=4.9), 3.34 (dt, 2H, J=1.7, J=3.2), 2.62 (dd, 2H, J=5.8, J=18.0), 2.13 (d, 2H, J=17.0); 1 3 C NMR (CD 3 0D): 6 217.62, 73.91, 43.91; LRCIMS: 116.9 (M+1). 25 (+)-(R)-4-Hydroxycyclopent-2-en-1-one (35) (79%); 1H NMR (CDC1 3 ): 6 7.61 (dd, 1H, J=2.3, J=5.6), 6.25 (dd, 1H, J=1.3, J=5.7), 5.08 (m, 1H), 2.80 (dd, 1H, J=6.1, J=18.5), 2.30 (dd, 1H, J=2.2, J=18.5) 1 3 C-NMR (CDC1 3 ): 6 207.8, 164.4, 134.5, 70.0, 44.1; [MD = +88.31 ee ~ 98%; LRCIMS: 99.0 (M+1). 30 The synthesis of the compounds shown in Scheme 1 will now be described.

WO 2006/000043 PCT/AU2005/000928 - 18 2,5-Dihydro-2,5-dimethoxy-2-methylfuran (1) To a mechanically stirred mixture of 2-methylfuran (18.2g, 222mol), Na 2

CO

3 (47.Og, 443mol, 2.02 equiv) and 170ml of methanol at -55'C was added a solution of bromine 5 (35.4g, 222mol, 1 equiv) in CH 2 C1 2 (12ml) over a one hour period. The reaction mixture was allowed to warm to 10 C over three hours, then filtered through celite. The filtrate was then mixed with brine (200ml) and extracted with CH 2 Cl 2 (1 x 200ml portion, 5 x 100ml portions). The combined organic fractions were dried, filtered and concentrated in vacuo to give 2,5-dihydro-2,5-dimethoxy-2-methylfuran (24.9g 145mmol, 79%) as a 10 yellow oil. 1H NMR (major isomer, CDCl 3 ): 6 5.9-6.0 (in, 2H), 5.47 (s, 1H), 3.49 (s, 3H), 3.19 (s, 3H), 1.50 (s, 3H); 1 H NMR (minor isomer, CDCl 3 ): 6 5.9-6.0 (in, 2H), 5.74 (s, 1H), 3.41 (s, 3H), 3.10 (s, 3H), 1.58 (s, 3H); 13 C NMR 6 134.4, 134.0, 130.1, 129.7, 112.7, 111.5, 107.7, 106.7, 55.5, 54.2, 49.9, 49.3, 26.1, 25.7. 15 (±)-4-Hydroxycyclopent-2-en-1-one (2) To a stirred deoxygenated solution of 2,5-dihydro-2,5-dimethoxy-2-methylfuran (1) (lOg, 69.4mmol) and hydroquinone (50mg) in water (278ml) at 0 0 C was added acetic acid (0.84g, 14mmol, 0.2 equiv). After one hour a solution of Na 2

HPO

4 .7H 2 0 (18.6g, 69.4mmol, 1 equiv) in water (60ml) was added and the mixture heated to 60'C for two 20 hours. Non-polar side products were removed by washing with hexanes (100ml) and the aqueous layer extracted with 1-butanol (7 x 100ml). The combined fractions were concentrated under reduced pressure to give a brown oil which was purified by flash chromatography using ethyl acetate:hexane (2:1) as the eluant on silica gel to give (±) 4-hydroxycyclopent-2-en-1-one as a yellow oil (42%). 'H-NMR (CDCl 3 ): 6 7.63 (dd, 25 1H, J=2.4, 5.6), 6.21 (dd, 1H, J=1.3, 5.7), 4.25 (d, 1H), 5.02-5.05 (in, 1H), 2.76 (dd, 1H, J=6.4, 18.5), 2.27 (dd, 1H, J=2.1, 18.7); ' 3 C-NMR (CDCl 3 ): 6 207.8, 164.4, 134.5, 70.0, 44.1; LRCIMS: 99.0 (M+1). The following reactions of Scheme 1 are described using (+)-4-hydroxycyclopent-2-en 30 1-one (2) as a reagent. However, as would clearly be understood by a person skilled in the art, these reactions could also be performed using either (+)-(R)-4 hydroxycyclopent-2-en-1-one (35) or (-)-(S)-4-hydroxycyclopent-2-en-1-one (27) to obtain an enantiopure product. The characteristics of the enantiopure compounds WO 2006/000043 PCT/AU2005/000928 - 19 synthesised by such methods are listed following the description of the synthesis of the respective compounds shown in Scheme 1. ( )-4-tert-Butyldimethylsiloxycyclopent-2-en-1-one (3) 5 To a stirred solution of 4-hydroxycylcopent-2-en-1-one (2) (1.66g, 16.88 mmol), dimethylaminopyridine (0.206g, 10 mol%) in dry dichloromethane (33ml) at 0 0 C under inert atmosphere, a solution of tert-butyldimethylsilylchloride (3.13g, 20.68 mmol, 1.2 equiv) in dry dichloromethane (1 lml) was added dropwise over ten minutes. The solution was allowed to warm to room temperature and stirred for 3 hours, after which 10 time 100ml of deionized water was added. The organic layer was separated, the aqueous phase extracted with dichloromethane (3 x 50ml) and the combined organic fractions dried with magnesium sulphate and concentrated in vacuo. The resulting oil was filtered using a short column of silica gel eluted with 10% ethyl acetate in petroleum ether. The fractions containing the product were concentrated in vacuo and then distilled under 15 high vacuum to give (±)-4-tert-butyldimethylsiloxycyclopent-2-en-1-one as a colourless oil (2.15g, 14.35mmol, 85%). 1 H NMR (CDCl 3 ): 8 7.33 (dd, 1H, J=2.3, J=5.7), 6.06 (dd, 1H, J=1.3, J=5.6), 4.86 (m, 1H), 2.59 (dd, 1H, J=5.9, J=18.2), 2.12 (dd, 1H, J=2.3, J=18.2), 0.79 (s, 1H), 0.01 (d, 1H, J=3.6); 13 C NMR (CDCl 3 ): 8 164, 135, 71.3, 45.5, 40.5, 25.5, 18.5, -4.43; GCMS:single peak @ 5.96minutes m/z: 213.0 (M+1). 20 (-)-(S)-4-tert-Butyldimethylsiloxycyclopent-2-en-1-one 1 H NMR (CDCl 3 ): 8 7.33 (dd, 1H, J=2.3, J=5.7), 6.06 (dd, 1H, J=1.3, J=5.6), 4.86 (m, 1H), 2.59 (dd, 1H, J=5.9, J=18.2), 2.12 (dd, 1H, J=2.3, J=18.2), 0.79 (s, 1H), 0.01 (d, 1H, J=3.6); 13C NMR (CDC1 3 ): 6 164.08, 134.69, 71.12, 45.23, 40.51, 25.99, 18.34, 25 4.44; GCMS: single peak @ 5.95 minutes m/z: 212.9 (M+1); [a1D -64.7 (c=1.3, MeOH). (+)-(R)-4-tert-Butyldimethylsiloxycyclopent-2-en-1-one H NMR (CDCl 3 ): a, 7.48 (dd, 1H, J=2.3, J=5.7), 6.21 (dd, 1H, J=1.3, J=5.7), 5.02 (m, 30 1H), 2.74 (dd, 1H, J=6.0, J=18.2), 2.27 (dd, 1H, J=2.3, J=18.2), 0.94 (s, 9H), 0.16 (d, 6H, J=3.5); "C NMR (CDCl 3 ): 8 164.18, 134.62, 71.03, 45.27, 40.51, 25.93, 18.31, 4.46; GCMS:213.0 (M+1); [a]D = +59.8 (c=0.5, MeOH).

WO 2006/000043 PCT/AU2005/000928 - 20 (±)-4-tert-Butyldimethylsiloxycyclopent-1-en-1-yl-trifluoromethanesulfonate (4) To a solution of L-selectride (1M in THF, 4.7ml, 4.7mmol) in anhydrous THF (35ml) at -78'C under nitrogen was added drop wise a solution of 4-tert butyldimethylsiloxycyclopent-2-en- 1 -one (3) (1.0g, 4.7mmol) and triethylamine (0.2ml) 5 in THF (15ml) over 30 minutes. After an additional 30 minutes, n-phenyl triflimide (1.5g, 4.1mmol) was added in two portions. The resulting solution gradually warmed to room temperature overnight, the solvent removed in vacuo and the residue partitioned between saturated sodium bicarbonate solution (50ml) and petroleum ether (100ml) overnight. The aqueous layer was extracted with petroleum ether (2 x 25ml) and the 10 combined organic fractions were washed with brine, dried with magnesium sulphate and concentrated in vacuo. The residue was then purified via flash chromatography using 1% triethylamine and 1 %ethylacetate in petroleum ether as the eluent on silica gel to give (±)-4-tert-butyldimethylsiloxycyclopent- 1-en-1 -yl-trifluoromethanesulfonate as a colourless oil (1.59g, 98%). 'H NMR (CDCl 3 ): 8 5.58 (m, 1H), 4.60 (tt, 1H, J=3.9, 15 J=7.3), 2.86 (dddd, 1H, J=2.1, J=3.4, J=7.3, J=16.3), 2.73 (ddd, 1H, J=1.2, J=7.1, J=16.5), 2.56 (dtd, 1H, J=2.0, J=4.0, J=16.3), 2.37 (m, 1H), 0.92 (s, 9H), 0.10 (s, 6H);

'

3 C NMR (CDCl 3 ): 6 146.66, 118.78 (q, J=320.8), 115.59, 69.81, 41.46, 39.29, 25.97, 18.26, -4.63; GCMS:single peak @ 6.38minutes m/z: 346.8 (M+1). 20 (+)-(R)-4-tert-Butyldimethylsiloxycyclopent-1-en-1-yl-trifluoromethanesulfonate 'H NMR (CDCl 3 ): 5 5.58 (m, 1H), 4.60 (tt, 1H, J=3.9, J=7.3), 2.86 (dddd, 1H, J=2.1, J=3.4, J=7.3, J=16.3), 2.73 (ddd, 1H, J=1.2, J=7.1, J=16.5), 2.56 (dtd, 1H, J=2.0, J=4.0, J=16.3), 2.37 (m, 1H), 0.92 (s, 9H), 0.10 (s, 6H); "C NMR (CDCl 3 ): 6 146.59, 118.69 (q, J=380.8), 115.38, 69.69, 41.29, 39.16, 25.75, -4.41; GCMS:346.8 (M+1) [a]D 25 +1.97 (c=1.01, MeOH). (-)-(S)-4-tert-Butyldimethylsiloxycyclopent-1-en-1-yl-trifluoromethanesulfonate 'H NMR (CDCl 3 ): 6 5.58 (m, 1H), 4.60 (tt, 1H, J=3.8, J=7.4), 2.86 (dddd, 1H, J=2.1, J=3.5, J=7.3, J=16.3), 2.73 (dd, 1H, J=7.1, J=16.5), 2.55 (qdd, 1H, J=2.0, J=4.0, 30 J=16.3), 2.37 (d, 1H, J=16.3), 0.92 (s, 9H), 0.10 (s, 6H); 1 3 C NMR (CDCl 3 ): 6 146.65, 118.78 (q, J=320.6), 115.60, 69.81, 41.46, 39.29, 25.98, 18.26,.-4.62; GCCIMS: rt single peak @ 6.40 minutes m/z: 346.7 (M+1); [a]D = -1.92 (c=1.3, MeOH).

WO 2006/000043 PCT/AU2005/000928 - 21 The synthesis of various phosphinates to be used in the synthesis of compounds (5) to (9) from compound (4), as shown in Schedule 1, will now be described. Ethyl 1,1-diethoxyethylphosphinate 5 Aqueous phosphinic acid was concentrated in vacuo at a temperature of less than 40'C to give at least 95% pure acid, which slowly crystallized upon standing. Triethyl orthoactetate (200ml) was cooled to 5'C under nitrogen, and boron trifluoride diethyletherate (5ml) was added slowly. The mixture was further cooled to -5'C and the phosphinic acid (16.3g) was added slowly. Temperature was precisely maintained at 10 -5'C during the addition. The mixture was then warmed to room temperature (r.t.) over 3 hours. Dihydrogen sodium phosphate solution (1.2M, 50ml) was then added in one portion with stirring. The solution was extracted with dichloromethane (2x50ml). The combined organic layers where then washed with water, dried using Mg 2

SO

4 and the solvent was removed in vacuo at a temperature of less than 40'C. The product was then 15 used without further purification in the next step (i.e. the reaction with compound (4)). 1 H NMR (CDCl 3 ): 5 6.95 (d, 1H, J=543.8), 1.50 (d, 3H, J=12.6), 1.39 (t, 3H, J=7.1), 1.24 (dt, 6H, J=2.2, J=4.9), 4.23 (m, 2H), 3.71 (m, 4H); "C NMR (CDCl 3 ): 8 100.36 (d, PC (OCH 2

CH

3

)

2

CH

3 , JPc=150.6), 63.36 (d, POC, 2 Jpoc=7.8), 57.96 (d, PC (OCCH 3

)

2 , 3 JPcoc=8.8), 19.18 (d, POCCH 3 , 3Jpocc=13.1), 16.58 (d, PC (OCCH 3

)

2 , 4 Jpcocc=5.6), 20 16.43 (d, PCCH 3 , 2 Jpcc=l04.4). MS data was not collected for phosphinates due to the extensive characterization of subsequent coupling products. 25 Ethyl 1,1-diethoxyethyl(methyl)phosphinate (alkylation of ethyl 1,1 diethoxyethylphosphinate) To a solution of NaH (1.6g, 40mmol) in THF (1Oml) was added slowly a solution of ethyl 1,1-diethoxyethylphosphinate (7.0g, 33mmol) in THF (10ml) under N 2 at r.t. The temperature was kept below 30'C during addition. The solution was stirred at r.t. for a 30 further 2 hours at which time ethyl iodide (14.18g, 99mmol) was added slowly. The solution was stirred for an additional 24 hours. The solution was cooled on an ice bath and treated carefully with water. The solution was concentrated in vacuo before being partitioned between water and DCM The DCM layer was dried with Mg 2

SO

4 and concentrated in vacuo. The product was distilled at high vacuum. IH NMR (CDCl 3 ): 6 WO 2006/000043 PCT/AU2005/000928 - 22 4.16 (m, 2H), 3.70 (m, 4H), 1.50 (d, 3H, J=11.3), 1.47 (d, 3H, J=13.8), 1.33 (t, 3H, J=7.1), 1.22 (t, 6H, J=7.1); 13 C NMR (CDC1 3 ): 8 101.15 (d, PC (OCH 2

CH

3

)

2

CH

3 , Jpc=143.1), 61.76 (t, POC, 2 Jpoc=5.7), 58.26 (d, PC (OCCH 3

)

2 , 3 Jpcoc=5.4), 20.61 (d,

POCCH

3 , 3 Jpocc=12.6), 16.89 (d, PC (OCCH 3

)

2 , 4 JpCocc=5.6), 15.66 (d, PCCH 3 , 5 2 Jpcc=13.9), 11.83 (d, PCH 3 , Jpc=88.7). Ethyl 1,1-diethoxyethyl(ethyl)phosphinate 1H NMR (CDC1 3 ): 8 4.19 (m, 2H) 3.70 (m, 4H) 1.76 (m, 2H) 1.50 (d, 3H, J=11.0) 1.32 (m, 3H) 1.21 (m, 9H); 13 C NMR (CDC1 3 ): 8 101.47 (d, PC (OCH 2

CH

3

)

2

CH

3 , 10 Jpc=137.5), 61.62 (d, POC, 2 Jpoc=6.5), 58.30 (d, PC (OCCH 3

)

2 , 3 Jpcoc=4.7), 26.31 (d,

PCH

2

CH

3 , Jpc=40.4), 20.79 (d, POCCH 3 , 3 JpoC=12.4), 16.70 (d, PC (OCCH 3

)

2 , 4 Jpcocc=6.0), 15.65 (d, PCCH 3 , 2 Jpcc=l8.8), 13.81 (d, PCH 2

CH

3 , 2 Jpec=5.9). Ethyl 1,1-diethoxyethyl(isopropyl)phosphinate 15 1H NMR (CDC1 3 ): 8 4.20 (m, 2H), 3.72 (m, 4H), 2.00 (m, 1H), 1.52 (d, 3H, J=1 0.8), 1.31 (t, 6H, J=7.1), 1.20 (m, 9H); 13 C NMR (CDC1 3 ): 8 102.00 (d, PC (OCH 2

CH

3

)

2

CH

3 , JPc=132.3), 61.57 (d, POC, 2 Jpoc=7.1), 58.27 (d, PC (OCCH 3

)

2 , 3 Jpcoc=4.5), 26.12 (d, PC (CH 3

)

2 , Jpc=86.5), 20.99 (d, POCCH 3 , 3 JpoCC12.4), 16.93 (d, PC (OCCH 3

)

2 , 4 Jpcocc=5.1), 15.93 (d, PC (CH 3

)

2 , 2 Jpec=5.3), 15.62 (d, PCCH 3 , 2 Jpcc=l8.4). 20 Ethyl 1,1-diethoxyethyl(butyl)phosphinate 'H NMR (CDC1 3 ): 8 4.19 (m, 2H), 3.71 (m, 4H), 1.72 (m, 4H), 1.51 (d, 3H, J=11.1), 1.42 (m, 2H), 1.33 (t, 3H, J=7.1), 1.22 (t, 6H, J=7.1), 0.94 (t, 3H, J=7.3); 1 3 C-NMR (CDC1 3 ): 8 102.34 (d, PC (OCH 2

CH

3

)

2

CH

3 , Jpc131.1), 62.84 (d, POC, 3 Jpoc=7.0), 25 57.21 (d, PC (OCCH 3

)

2 , 3 Jpcoc=5.1), 28.48 (d, PCH 2

(CH

2

)

2

CH

3 , Jpc=93.8), 23.75 (d,

PCH

2

CH

2

CH

2

CH

3 , 2JpcC=16.1), 22.92 (d, P(CH 2

)

2

CH

2

CH

3 , JPCCC=3-0), 18.60 (d,

POCH

2

CH

3 , 3 Jpoccl 3.4), 16.83 (d, PC (OCCH 3

)

2 , 4 Jpcocc=4.3), 15.31 (d, PCCH 3 , 2 Jpcc=17.7), 13.76 (P(CH2)3CH 3 ). 30 Ethyl 1,1-diethoxyethyl(phenyl)phosphinate 1 H NMR (CDC1 3 ): 8 7.36 (m, 5H), 4.12 (m, 211), 3.70 (m, 4H), 1.50 (d, 3H, J=11.2), 1.25 (m, 6H), 1.21 (t, 3H, J=7.1).

WO 2006/000043 PCT/AU2005/000928 - 23 Ethyl methylphosphinate (hydrolysis of alkyl(1,1-diethoxyethyl)phosphinates) To a solution of ethyl 1,1-diethoxyethyl(methyl)phosphinate (3.7g, l7mmol) in DCM: 10% EtOH (60ml), chlorotrimtheylsilane (2.51 g, 23. 1mmol) was added dropwise at r.t. The solution was then stirred for 24hours at r.t. before the volatile components were 5 removed in vacuo. The product was used in the next step (i.e. the reaction with compound (4)) without further purification. 'H NMR (CDCl 3 ): 8 7.28 (d, 1H, J=552.6), 4.14 (m, 2H), 1.58 (dd, 3H, J=1.8, J=15.3), 1.36 (t, 3H, J=7.1); 13 C NMR (CDCl 3 ): 6 62.44 (dd, POC, 2 Jpoc=6.3, J=61.7), 16.51 (d, POCCH 3 , 3 Jpocc=9.4), 11.29 (d, PCH 3 , Jrc=144.3). 10 Ethyl ethylphosphinate 'H NMR (CDCl 3 ): 8 7.08 (dt, 1H, J=1.9, J=533.7), 4.16 (m, 2H), 1.83 (m, 2H), 1.37 (t, 3H, J=7.1), 1.17 (td, 3H, J=7.8, J=21.5); 13 C NMR (CDCl 3 ): 6 62.92 (d, POC, 3 Joc=7.1), 21.83 (d, PCH 2

CH

3 , Jrc= 9 4

.

7 ), 16.47 (d, POCCH 3 , 3 Jpocc=6.1), 4.85 (d, 15 PCH 2

CH

3 , 2 Jpcc=4.0). Ethyl isopropylphosphinate 1 H NMR (CDCl 3 ): 6 6.88 (dd, 1H, J=1.3, J=521.6), 4.15 (m, 2H), 1.92 (dtt, 1H, J=1.0, J=7.1, J=14.6), 1.36 (t, 3H, J=7.0), 1.17 (ddd, 1H, J=1.1, J=7.2, J=19.7); 1 3 C NMR 20 (CDCl 3 ): 6 63.39 (d, POC, 2 Joc=7.6), 27.26 (d, PC (CH 3

)

2 , Jrc= 9 5.

3 ), 16.44 (d,

POCCH

3 , 3 Jpocc=5.9), 14.26 (dd, PC(CH 3

)

2 , J1.6, J=11.4). Ethyl butylphosphinate 1 H NMR (CDCl 3 ): 6 7.11 (d, 1H, J=534.7), 4.14 (m, 2H), 1.81 (m, 2H), 1.57 (m, 2H), 25 1.43 (m, 2H), 1.27 (t, 3H, J=7.1), 0.92 (t, 3H, J=7.2); 1 3 C NMR (CDCl 3 ): 6 62.84 (d, POC, 2 joc=7.0), 28.48 (d, PCH 2

(CH

2

)

2

CH

3 , JPC= 93

.

8 ), 23.75 (d, PCH 2

CH

2

CH

2

CH

3 , 2 Jcc=16.1), 22.92 (d, P(CH 2

)

2

CH

2

CH

3 , 3 Jpccc=3.0), 16.60 (d, POCH 2

CH

3 , 3 JoCC13.4), 13.76 (P(CH 2

)

3

CH

3 ). 30 Ethyl phenylphosphinate iH NMR (CDCl 3 ): 6 7.34 (m, 5H), 7.10 (d, 1H, J=551.0), 4.11 (m, 2H), 1.27 (t, 3H, J=7.1).

WO 2006/000043 PCT/AU2005/000928 - 24 ( )-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)methylphosphinate (5) (palladium catalysed C-P bond formation) To a solution of DABCO (200mg, 2.Ommol, 3 equiv), methylphosphinate (94mg, 0.435mmol, 1.5 equiv) and 4-tert-butyldimethylsiloxycyclopent-1-en-1-yl 5 trifluoromethanesulfonate (4) (200mg, 0.58 mmol) in toluene (10ml) was added tetrakis- (triphenylphosphine)palladium(0) (17mg, 2.5 mol%). The solution was stirred at room temperature for 18 hours at which time a second portion of tetrakis (triphenylphosphine)palladium(0) (10mg, 2.5 mol%) was added. The solution was stirred for a further 24 hours, the toluene removed in vacuo and the residue purified via 10 flash chromatography using ethylacetate: 10% ethanol as the eluent on silica gel to give ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)methylphosphinate as a colourless oil (143mg, 78%).

1 H NMR (CDCl 3 ): 8 6.62 (ddm, 1H, J=10.8, J=17.8), 4.63 (m, 1H), 4.10 (m, 2H), 2.72 (m, 2H), 2.45 (m, 2H), 1.49 (d, 3H, J=17.5), 1.34 (t, 3H, J=7.1), 0.88 (d, 9H, J=2.6), 0.07 (d, 6H, J=1.3); "C NMR (CDCl 3 ): 8 145.44 and 144.83 (2d from 2 15 diastereomers, C (2), 2 Jpcc=11.5), 2 Jpcc=10.63) 134.28 (d, C (1), Jpc=124.3), 72.99 and 72.94 (2d from 2 diastereomers, C (4), 3 Jpccc=11.6, 3 jpCC=l 1.4), 61.77 (d, POCH 2

CH

3 , 2 Jpoc=6.3), 44.48 and 44.43 (2d from 2 diastereomers, C (5), 2JpcC=16.3, 2Jpcc=15.7), 43.33 (d, C (3), 3 Jpccc=l2.1), 25.92 (SiC (CH3)3), 18.25 (SiC (CH 3

)

3 ), 16.73 and 16.62 (2d from 2 diastereomers, POCH 2

CH

3 , 3 Jpocc=6.2, 3 Jpocc=6.7), 11.40 (d, PCH 3 , 20 Jcp=144.4), -4.55 (Si (CH 3

)

2 ); HREIMS: for C 14

H

29 0 3 PSi calculated (M): 304.1624 observed: 304.1631; GCCIMS: rt = single peak @ 10.07 minutes m/z: 305.1 (M+1). (-)-(R)-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)methylphosphinate Obtained as a colourless oil (79%).'H-NMR (CDCl 3 ): 8 6.62 (ddm, 1H, J=10.8, 25 J=17.8), 4.63 (m, 1H), 4.10 (m, 2H), 2.72 (m, 2H), 2.45 (m, 2H), 1.49 (d, 3H, J=17.5), 1.34 (t, 3H, J=7.1), 0.88 (d, 9H, J=2.6), 0.07 (d, 6H, J=1.3); 13 C-NMR (CDCl 3 ): 6 145.44 and 144.83 (2d from 2 diastereomers, C (2), 2 Jpcc=11.5), 2 Jec=10.63) 134.28 (d, C (1), Jpc=124.3), 72.99 and 72.94 (2d from 2 diastereomers, C (4), 3 JpccC=11.6, 3 JpCCC 11.4), 61.77 (d, POCH 2

CH

3 , 2 Jpoc=6.3), 44.48 and 44.43 (2d from 2 30 diastereomers, C (5), 2 JrcC=16.3, 2 Jpcc=15.7), 43.33 (d, C (3), 3 Jpccc=12.1), 25.92 (SiC (CH3)3), 18.25 (SiC (CH 3

)

3 ), 16.73 and 16.62 (2d from 2 diastereomers, POCH 2

CH

3 , 3 JPocc6.2, 3 Jpocc6.7), 11.40 (d, PCH 3 , JCP=144.4), -4.55 (Si (CH 3

)

2 ); [cX]D =-5.40; GCCIMS: rt = single peak @ 10.09 minutes m/z: 305.1 (M+1).

WO 2006/000043 PCT/AU2005/000928 - 25 (+)-(S)-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)methylphosphinate Obtained as a colourless oil (96%). 1H NMR (CDCl 3 ): 8 6.62 (tdd, 1H, J=2.0, J=10.9, J=17.8), 4.64 (m, 1H), 4.10 (m, 2H), 2.74 (m, 2H), 2.45 (m, 2H), 1.49 (d, 3H, J=17.5), 5 1.34 (t, 3H, J=7.1), 0.89 (d, 9H, J=2.6), 0.08 (d, 6H, J=1.4); ' 3 C-NMR (CDCl 3 ): 8 145.44 and 144.83 (2d from 2 diastereomers, C (2), 2 Jpcc=11.5), 2 Jpcc=10.63) 134.28 (d, C (1), Jpc=124.3), 72.99 and 72.94 (2d from 2 diastereomers, C (4), 3 Jpccc=11.6, 3 Jpccc=l 1.4), 61.77 (d, POCH2CH 3 , 2 Jpoc=6.3), 44.48 and 44.43 (2d from 2 diastereomers, C (5), 2 Jrcc=16.3, 2 jpCc=15.7), 43.33 (d, C (3), 3 Jpccc=12.1), 25.92 (SiC 10 (CH3)3), 18.25 (SiC (CH 3

)

3 ), 16.73 and 16.62 (2d from 2 diastereomers, POCH 2

CH

3 , 3 Jpocc=6.2, 3 Jpocc=6.7), 11.40 (d, PCH 3 , JcP=144.4), -4.55 (Si (CH 3

)

2 ); GCCIMS: rt = single peak @ 10.11 minutes m/z: 305.0 (M+1). A similar procedure was used to prepare compounds (6) to (9). The characteristics of 15 these compounds, as well as the enantiopure compounds corresponding to compound (8), are described below. (±)-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)ethylphosphinate (6) Obtained as a colourless oil (76%). 1H NMR (CDC1 3 ): 8 6.65 (m, 1H), 4.62 (m, 1H), 20 4.11 (m, 2H), 2.74 (m, 2H), 2.48 (m, 2H), 1.76 (m, 2H), 1.23 (m, 6H), 0.89 (dd, 9H, J=0.5, J=2.0), 0.08 (s, 1H); "C NMR (CDCl 3 ):S 145.88 (t, C (2), 2 Jpcc=10.7), 133.07 (d, C (1), Jcp=123.6), 73.05 and 73.04 (2d from 2 diastereomers, C (4), 3 Jpccc=10.9, 3 Jpccc=l0.9), 61.71 (d, POCH 2

CH

3 , 2 Jpoc=6.5), 44.55 and 44.47 (2d from 2 diastereomers, C (5), 2 JpcC=15.3), 43.83 and 43.67 (2d from 2 diastereomers, C (5), 25 3 Jpccc=9.2, 3 JpCcc=8.9), 25.91 (SiC (CH3)3), 21.47 (d, PCH 2

CH

3 , Jpcl102.6), 16.71 (t,

POCH

2

CH

3 , J=6.1), 6.79 (d, PCH 2

CH

3 , J=6.8); GCMS: (m/z) 319.1 (M+1); HREIMS: for C, 5

H

31 0 3 PSi calculated (M): 318.1780 observed: 318.1789; GCC]MS: rt: single peak @ 10.53 minutes m/z: 319.1 (M+1). 30 ( )-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)isopropylphosphinate (7) Obtained as colourless needles (90%). iH NMR (CD 3 0D): 8 6.71 (dm, 1H, J=9.9), 4.69 (m, 1H), 4.08 (m, 2H), 2.81 (m, 2H), 2.48 (m, 2H), 2.01 (m, 1H), 1.34 (t, 3H, J=7.1), 1.20 (dd, 6H, J=7.2, J=18.7), 0.92 (d, J=0.64, 9H), 0.12 (s, 6H); 1 3 C NMR (CD 3 0D): 5 WO 2006/000043 PCT/AU2005/000928 - 26 147.57 (triplet, C (2), J=9.6), 131.55 and 135.41 (2d from 2 diastereomers, C (1), Jcp=121.0, Jcpl121.1), 72.88 (d, C (4), 3 JPCCC=10-8), 60.91 and 60.87 (2d from 2 diastereomers, POCH 2

CH

3 , 2 Jroc=7.0, 2 Jpoc=7.0), 44.41 and 44.34 (2d from 2 diastereomers, C (5), 2 JpCC=l5.2, 2 Jcc=15.3), 44.04 and 43.90 (2d from 2 5 diastereomers, C (3), 3 Jpccc=11.3, 3 Jpccc=l1.1), 26.81 and 26.64 (2d from 2 diastereomers, PCH (CH 3

)

2 , Jcp 103.2, Jcp=102.9), 25.11 (SiC (CH 3

)

2 ), 17.67 (SiC

(CH

3

)

2 ), 15.68 (d, POCH 2

CH

3 , 3 Jpocc=6.0), 13.77 and 13.72 (d, PCH (CH 3

)

2 , 2 Jpcc=6.1, 2 Jcc=6.2), -5.82 (Si (CH 3

)

2 ); GCCIMS: rt: 2 peaks from 2 diastereomers @ 10.67 and 10.73 minutes m/z: 333.1 (M+1). 10 ( )-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)butylphosphinate (8) Obtained as colourless needles (94%). 'H NMR (CD 3 0D): 8 6.69 (dm, 1H, J=10.7), 4.69 (m, 1H), 4.06 (m, 2H), 2.82 (m, 2H), 2.47 (m, 2H), 1.82 (m, 2H), 1.54 (m, 4H), 1.36 (t, 3H, J=3.0), 1.29 (t, 3H, J=6.7), 0.92 (d, 9H, J=1.2), 0.12 (s, 6H); 1 3 C NMR 15 (CD 3 0D): 5 146.60 (overlapping doublets, C (2), 2 JpCc=11.8), 132.54 (d, C (1), Jpc=1 2 4 .8), 72.82 (d, C (4), 3 Jpcc=l0.7), 60.79 and 60.74 (2d from 2 diastereomers,

POCH

2

CH

3 , 2 Jpoc=6.5, 2 Jpoc=6.6), 44.46 and 44.41 (2d from 2 diastereomers, C (5), 2jpcc=15.

8 , 2 Jpcc=15.8), 43.52 and 43.49 (2d from 2 diastereomers, C (3), 3 JPccC=12.1, 3 Jpccc=1 1.8), 27.17 and 26.92 (2d from 2 diastereomers, PCH 2

(CH

2

)

2

CH

3 , Jpc=101.

4 , 20 Jpc=100.

8 ), 25.13 (SiC (CH 3

)

2 ), 23.59 (d, P (CH 2

)

2 Ci1 2

CH

3 , Jpccc=23.9), 23.52 (d,

PCH

2

CH

2

CH

2

CH

3 , Jpcc=30.3), 17.68 (s, SiC (CH3)2), 15.67 and 15.59 (2d from 2 diastereomers, POCH 2

CH

3 , 3 Jpocc=9.0, 3 Jpocc=8.7), 12.76 (P (CH 2

)

3

CH

3 ), -5.84 (Si

(CH

3

)

2 ); HREIMS: for C1 7

H

35

O

3 PSi calculated (M): 346.2093 observed: 346.2096; GCCIMS: rt: 2 peaks from 2 diastereomers @ 11.45 and 11.49 minutes m/z: 347.1 25 (M+1). (R)-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)butylphosphinate Obtained as colourless needles (99%). 1 H-NMR (CD 3 0D): 5 6.69 (dm, 1H, J=10.7), 4.69 (m, 1H), 4.06 (m, 2H), 2.82 (m, 2H), 2.47 (m, 2H), 1.82 (m, 2H), 1.54 (in, 4H), 30 1.36 (t, 3H, J=3.0), 1.29 (t, 3H, J=6.7), 0.92 (d, 9H, J=1.2), 0.12 (s, 6H); 1 3 C-NMR

(CD

3 0D): 5 146.60 (overlapping doublets, C (2), 2 JpCc=11.8), 132.54 (d, C (1), Jpc=124.8), 72.82 (d, C (4), 3 Jpecc=10.7), 60.79 and 60.74 (2d from 2 diastereomers,

POCH

2

CH

3 , 2Jroc=6.5, 2 Jpoc=6.6), 44.46 and 44.41 (2d from 2 diastereomers, C (5), WO 2006/000043 PCT/AU2005/000928 - 27 2Jpcc=15.8, 2 Jpcc=15.8), 43.52 and 43.49 (2d from 2 diastereomers, C (3), 3 JpCCC=12.1, 3JpCCC 11.8), 27.17 and 26.92 (2d from 2 diastereomers, PCH 2

(CH

2

)

2

CH

3 , JPCl101.4, JPc=100.8), 25.13 (SiC (CH 3

)

2 ), 23.59 (d, P (CH 2

)

2

CH

2

CH

3 , 3 Jpccc=23.9), 23.52 (d,

PCH

2

CH

2

CH

2

CH

3 , Jpcc=30.3), 17.68 (s, SiC (CH 3

)

2 ), 15.67 and 15.59 (2d from 2 5 diastereomers, POCH 2

CH

3 , 3 Jpocc=9.0, 3 Jpocc=8.7), 12.76 (P (CH 2

)

3

CH

3 ), -5.84 (Si

(CH

3

)

2 ); [a]D =-2.38; GCCIMS: rt: 2 peaks from 2 diastereomers @ 11.46 and 11.51 minutes m/z: 347.1 (M+1). (S)-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)butylphosphinate 10 Obtained as colourless needles (92%). 'H-NMR (CD 3 0D): 8 6.69 (dm, 1H, J=10.7), 4.69 (in, 1H), 4.06 (in, 2H), 2.82 (in, 2H), 2.47 (in, 2H), 1.82 (in, 2H), 1.54 (in, 4H), 1.36 (t, 3H, J=3.0), 1.29 (t, 3H, J=6.7), 0.92 (d, 9H, J=1.2), 0.12 (s, 6H); 13 C-NMR

(CD

3 0D) 8 146.60 (overlapping doublets, C (2), 2 JPcC=11.8), 132.54 (d, C (1), Jpc=124.8), 72.82 (d, C (4), 3 JpCcc=10.7), 60.79 and 60.74 (2d from 2 diastereomers, 15 POCII 2

CH

3 , 2 Jpoc=6.5, 2 Jpoc=6.6), 44.46 and 44.41 (2d from 2 diastereomers, C (5), 2JpCc=15.8, 2 Jpcc=l5.8), 43.52 and 43.49 (2d from 2 diastereomers, C (3), 3 Jpccc=12.1, 3 Jpccc=11.8), 27.17 and 26.92 (2d from 2 diastereomers, PCH 2

(CH

2

)

2

CH

3 , Jc=101.4, JPc=100.8), 25.13 (SiC (CH 3

)

2 ), 23.59 (d, P (CH 2

)

2

CH

2

CH

3 , 3 Jpccc=23.9), 23.52 (d,

PCH

2

CH

2

CH

2

CH

3 , Jpcc=30.3), 17.68 (s, SiC (CH3)2), 15.67 and 15.59 (2d from 2 20 diastereomers, POCH 2

CH

3 , 3 JPocc=9.0, 3 Jpocc=8.7), 12.76 (P (CH 2

)

3

CH

3 ), -5.84 (Si

(CH

3

)

2 ); GCCIMS: rt: 2 peaks from 2 diastereomers @ 11.46 and 11.51 minutes m/z: 347.1 (M+1) ( )-Ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)benzylphosphinate (9) 25 Obtained as a colourless oil. 1 H NMR (CDCl 3 ): 8 0.09 (s, 6), 0.90 (s, 9) 1.29 (t, 3, J=7.0), 2.45 (in, 2), 2.76 (in, 2), 3.95 (in, 2), 4.65 (in, 1), 6.55 (bd, 1, J=18.0), 7.1-7.5 (in, 5). (d)-Ethyl(4-hydroxycyclopent-1-enyl)methylphosphinate (10) (deprotection of tert 30 butyldimethylsilyl protected alcohol) To a solution of ethyl(4-tert-butyldimethylsiloxycyclopent-1-enyl)methylphosphinate (5) (350mg, 1.2mmol,1 equiv) under nitrogen was added tert-butylammoniumfluoride (1M in THF, 1.44ml, 1.2 equiv). The solution was stirred at room temperature for 12 hours and the solvent was removed in vacuo. The residue was purified by flash WO 2006/000043 PCT/AU2005/000928 - 28 chromatography using ethylacetate:ethanol (75:15) as the eluant on silica gel to give ethyl(4-hydroxycyclopent-1-enyl)methylphosphinate as a yellow oil (208mg, 98%). 'H NMR (CDC1 3 ): 6 6.62 (d, 1H, J=10.6), 4.65 (m, 1H), 4.02 (m, 2H), 3.04 (m, 1H), 2.82 (d, 1H, J=16.5), 2.55 (d, 1H, J=18.0), 1.54 (dd, 3H, J=4.3, J=14.5), 1.33 (dt, 3H, J=2.0, 5 J=7.1); 1 3 C NMR (CDCl 3 ): 5 145.63 and 145.51 (2d from 2 diastereomers, C (2), 2Jpcc=11.4, 2 jPcC =11.8), 133.50 (d, C (1), Jcp=131.6), 71.27 (d, C (4), 3 Jpccc=l1.2), 60.87 and 60.85 (dd, POCH 2

CH

3 , 2 Jpoc=6.3, 2Jpoc=6.3), 43.65 (d, C (5), 2 Jpcc=16.4), 42.53 and 432.45 (2d from 2 diastereomers, C (3), 3 Jpccc=12.3, 3 Jpccc =12.1), 15.64 (d,

POCH

2

CIH

3 , 3 Jpocc=6.6), 12.74 and 12.57 (2d from 2 diastereomers, PCH 3 , JPC=102.5, 10 J=102.2); LREIMS: 190.1 (M). (R)-Ethyl(4-hydroxycyclopent-1-enyl)methylphosphinate 1 HNMR (CDCl 3 ): 8 6.61 (d, 1H, J=10.6), 4.64 (qdd, 1H, J=2.0, J=3.9, J=8.0), 4.00 (m, 2H), 2.78 (m, 2H), 2.54 (m, 2H), 1.53 (dd, 3H, J=4.5, J=14.5), 1.32 (dt, 3H, J=2.1, 15 J=7.1); 1 3 C-NMR (CDCl 3 ): 5 145.63 and 145.51 (2d from 2 diastereomers, C (2), 2 Jc=11.4, 2JpcC =11.8), 133.50 (d, C (1), Jcp=131.6), 71.27 (d, C (4), 3 Jccc=11.2), 60.87 and 60.85 (dd, POCH 2

CH

3 , 2 Jpoc=6.3, 2 Jpoc=6.3), 43.65 (d, C (5), 2 Jpcc=16.4), 42.53 and 432.45 (2d from 2 diastereomers, C (3), 3 Jpccc=12.3, 3 JPccc =12.1), 15.64 (d,

POCH

2

CH

3 , 3 Jpocc=6.6), 12.74 and 12.57 (2d from 2 diastereomers, PCH 3 , Jpc=102.5, 20 J=102.2); LREIMS: 190.1 (M). (S)-Ethyl(4-hydroxycyclopent-1-enyl)methylphosphinate 'H-NMR (CDCl 3 ): 5 6.61 (d, 1H, J=10.6), 4.64 (qdd, 1H, J=2.0, J=3.9, J=8.0), 4.00 (m, 2H), 2.78 (m, 2H), 2.54 (m, 2H), 1.53 (dd, 311, J=4.5, J=14.5), 1.32 (dt, 3H, J=2.1, 25 J=7.1); 1 3 C-NMR (CDCl 3 ): 5 145.63 and 145.51 (2d from 2 diastereomers, C (2), 2Jpcc=l1.4, 2JPcC =11.8), 133.50 (d, C (1), Jcp 1316), 71.27 (d, C (4), 3JpCCC 11.2), 60.87 and 60.85 (dd, POCH 2

CH

3 , 2 Jpoc=6.3, 2 Jpoc=6.3), 43.65 (d, C (5), 2 Jpcc=16.4), 42.53 and 432.45 (2d from 2 diastereomers, C (3), 3 Jpccc=12.3, 3 Jpccc =12.1), 15.64 (d,

POCH

2

CH

3 , 3 Jpocc=6.6), 12.74 and 12.57 (2d from 2 diastereomers, PCH 3 , Jpc=l0 2 .5, 30 J=102.2); LREIMS: 190.1 (M).

WO 2006/000043 PCT/AU2005/000928 - 29 A similar procedure was used to prepare compounds (11) to (14). The characteristics of these compounds, as well as the enantiopure compounds corresponding to compound (13), are described below. 5 (±)-Ethyl(4-hydroxycyclopent-1-enyl)ethylphosphinate (11) 1 H NMR (CDCl 3 ): 6 6.62 (dm, 1H, J=10.0), 4.64 (t, 1H, J=5.5), 4.02 (m, 2H), 2.86 (s, 1H), 2.78 (m, 2H), 2.53 (m, 2H), 1.78 (m, 2H), 1.32 (dt, 3H, J=2.0, J=7.1), 1.13 (dtd, 3H, J=2.2, J=7.7, J=18.6); 13 C NMR (CDCl 3 ): 6 145.55 and 145.46 (2d from 2 diastereomers, C (2), 2 Jpcc=l0.3, 2 Jpcc=10.2), 133.32 (d, C (1), Jpc=1 2 4

.

2 ), 72.00 (d, C 10 (4), 3 Jrccc=10.4), 60.64 and 60.61 (2d from 2 diastereomers, POCH 2

CH

3 , 2Joc= 6

.

4 , 2Jpoc =6.4), 44.39 (d, C (5), 2jrCC=15.6), 43.62 and 43.57 (2d from 2 diastereomers, C (3), 3 Jpccc =11.6, 3 JpccC=1 1.7), 21.40 and 21.37 (2d from 2 diastereomers, PCH 2

CH

3 , Jpc=101.

7 , Jpc=101.

4 ), 16.78 (d, POCH 2

CH

3 , 'lpocc=6.3), 5.85 (d, PCH 2

CH

3 , 2 Jpcc=4.8); LREIMS: 204.1 (M). 15 (±)-Ethyl(4-hydroxycyclopent-1-enyl)isopropylphosphinate (12) 1H NMR (CDCl 3 ): 6 6.64 (dm, 1H, J=9.2), 4.65 (m, 1H,), 4.05 (m, 2H), 2.80 (m, 2H), 2.60 (s, 1H), 2.53 (m, 2H), 1.93 (m, 1H), 1.33 (dt, 3H, J=1.9, J=7.0), 1.21 (d, 3H, J=7.2), 1.16 (d, 3H, J=7.1); 13 C NMR (CDCl 3 ): 6 146.08 (t, C (2), 2 Jpc=9.4), 132.72 (d, 20 C (1), Jpc= 119.9), 72.21 (d, C (4), 3 JpCcc=9.9), 60.73 and 60.71 (2d from 2 distereomers, POCH 2

CH

3 , 2Jpoc= 6

.

8 , J=6.8), 44.37 (d, C (5), 2Jpcc=15.

2 ), 44.23 and 44.14 (2d from 2 diastereoamers, C (3), 3 jpccc=1 1.0, J=11.1), 27.46 (d, POCH (CH 3

)

2 , Jpc=l0 2

.

3 ), 16.80 (d, POCH 2

CH

3 , 3 Jpocc=6.3), 15.40 and 15.37 (2d from 2 diastereomers, 2Jpec= 2 5

.

7 , 2JPcc= 2 8 .0); LREIMS: 218.1 (M). 25 ( )-Ethyl(4-hydroxycyclopent-1-enyl)butylphosphinate (13) (99%) 1H NMR (CDCl 3 ): 6 6.62 (dm, 1H, J=10.1), 4.64 (m, 1H), 4.08 (m, 2H), 2.81 (m, 2H), 2.53 (m, 2H), 1.75 (m, 2H), 1.56 (m, 2H), 1.41 (hept, 2H, J=7.3), 1.32 (dt, 3H, J=2.0, J=7.0), 0.92 (t, 1H, J=7.2); 13 C NMR (CDCl 3 ): 6 145.31 and 145.12 (2d from 2 30 diastereomers, C (2), 2 jpcc=10.7, 2 Jpcc=10.8), 133.76 (d, C (1), Jpc=125.

6 ), 72.01 (d, C (4), 3 JpccC=l0.5), 60.56 (d, POCH 2

CH

3 , 2 Joc=6.3), 44.38 (d, C (5), 2 Jrcc=15.6), 43.61 and 43.55 (2d from 2 diastereomers, C (3), 3 JrccC=1 1.6, 3 JPccc=l1.7), 28.14 (d, PCH 2

(CH

2

)

2

CH

3 , Jrc=100.

3 ), 23.99 (d, PCH 2

CH

2

CH

2

CH

3 , 2 Jpcc=16.3), 23.86 (d, P WO 2006/000043 PCT/AU2005/000928 - 30 (CH 2

)

2

CH

2

CH

3 , 3 Jpccc=3.7), 16.79 (d, POCH 2

CH

3 , 2Jpoc=6.3), 13.83 (P (CH 2

)

3

CH

3 ); LREIMS: 232.1. (R)-Ethyl(4-hydroxycyclopent-1-enyl)butylphosphinate 5 'H NMR (CDCl 3 ): 5 6.61 (m, 1H), 4.63 (m, 1H), 3.99 (m, 2H), 2.78 (m, 2H), 2.52 (m, 2H), 1.75 (m, 2H), 1.54 (ddt, 2H, J=6.7, J=9.6, J=16.3), 1.41 (m, 2H), 1.31 (t, 3H, J=7.1), 0.92 (t, 3H, J=7.2); 13 C NMR (CDC13): 6 145.36 and 145.16 (2d from 2 diastereomers, C (2), 2 jpce =11.0, 2 jrCC =10.7), 133.73 (d, C (1), Jpc =124.3), 72.04 (d, C (4), 3 Jpccc=10.4), 60.57 (d, POCH 2

CH

3 , 2 Jpoc=5.8), 44.38 (d, C (5), 2 JpcC=15.6), 10 43.56 and 43.61 (2d from 2 diastereomers, C (3), 3 Jpccc=11.7, 3 Jpecc =11.6), 28.13 (d,

PCH

2

(CH

2

)

2

CH

3 , Jpc=100.3), 24.10 (d, PCH 2

CH

2

CH

2

CH

3 , 2 jpcc=16.3), 23.73 (d, P

(CH

2

)

2

CH

2

CH

3 , 3 Jpccc=3.6), 16.78 (d, POCH 2

CH

3 , 2Jpoc=6.4), 13.82 (P (CH 2

)

3

CH

3 ); LREIMS: 232.1. 15 (S)-Ethyl(4-hydroxycyclopent-1-enyl)butylphosphinate 1 H-NMR (CDC1 3 ): 6 6.61 (m, 1H), 4.63 (m, 1H), 3.99 (m, 2H), 2.78 (m, 2H), 2.52 (m, 2H), 1.75 (m, 2H), 1.54 (ddt, 2H, J=6.7, J=9.6, J=16.3), 1.41 (m, 2H), 1.31 (t, 3H, J=7.1), 0.92 (t, 3H, J=7.2); 1 3 C-NMR (CDC1 3 ): 8 145.36 and 145.16 (2d from 2 diastereomers, C (2), 2 jcC = 11.0, 2 jpcC =10.7), 133.73 (d, C (1), Jpc =124.3), 72.04 (d, 20 C (4), 3 Jpccc=10.4), 60.57 (d, POCH 2

CH

3 , 2 Jpoc=5.8), 44.38 (d, C (5), 2 JpCc=15.6), 43.56 and 43.61 (2d from 2 diastereomers, C (3), 3 Jpccc=11.7, 3 jpccC =11.6), 28.13 (d,

PCH

2

(CH

2

)

2

CH

3 , JPc= 00.3), 24.10 (d, PCH 2

CH

2

CH

2

CH

3 , 2 Jpcc=16.3), 23.73 (d, P

(CH

2

)

2

CH

2

CH

3 , 3 Jpccc=3.6), 16.78 (d, POCH 2

CH

3 , 2Jpoc=6.4), 13.82 (P (CH 2

)

3

CH

3 ); LREIMS: 232.1. 25 ( )-Ethyl(4-hydroxycyclopent-1-enyl)benzylphosphinate (14) 1H NMR (CDCl 3 ): 6 1.29 (t, 3, J=7.1), 2.43 (m, 2), 2.72 (in, 2), 3.95 (m, 2), 4.53 (m, 1), 6.55 (bd, 1, J=18.0), 7.1-7.5 (m, 5). 30 ( )-(4-Aminocyclopent-1-enyl)methylphosphinic acid (15) (conversion of alcohol to amine via Mitsunobu/Staudinger reaction) To a solution of (±)-ethyl(4-hydroxycyclopent-1-enyl)methylphosphinate (10) (150mg, 0.85mmol), DIAD (0.7ml, 1.87mmol, 2.2 equiv) and HN 3 (1.9M in benzene, 1.lml, 1.7mmol, 2equiv) in anhydrous THF (1 Oml) at 0 0 C was added triphenylphosphine WO 2006/000043 PCT/AU2005/000928 - 31 (0.89g, 3.4mmol, 4 equiv) in small portions over 1 hour. The reaction mixture was allowed to warm to room temperature and stirred for 12 hours. The reaction mixture was then heated to 50'C for 3 hours at which time water (0.2ml) was added and the heating continued for a further 2 hours. The mixture was the cooled to room 5 temperature and the solvent removed in vacuo. The residue was separated between HCl (1M, 1 0ml) and DCM (1 Oml). The organic layer was separated and extracted with aqueous HCl (2 x 10ml). The combined aqueous layers were washed with DCM (2x1Oml) and concentrated in vacuo. The crude amino ester hydrochloride salt was hydrolysed by refluxing in aqueous HCl (6M, 15ml) for 30 hours after which time the 10 mixture was cooled to room temperature and the solvent removed in vacuo. The residue was purified by ion exchange chromatography (Dowex 50, He), eluting first with water until the eluant was neutral and colourless followed by pyridine (IM). Fractions containing the product were collected and concentrated in vacuo to give (±)-(4 aminocyclopent-1-enyl)methylphosphinic acid as a yellow solid (80mg, 64%).'H NMR 15 (D 2 0): 5 7.51 (in, 2H), 6.11 (d, 1H, J=9.8), 3.96 (in, 1H), 2.86 (in, 2H), 2.46 (in, 2H), 1.22 (d, 3H, J=14.1); 13C-NMR (D 2 0): 8 136.8 (d, C(2), 2 Jpcc=11.5), 135.56 (d, C (1), JPc=118.0), 51.0 (d, C(4), 3 Jccc=l0.3), 38.9 (d, C(3), 2 JpcC=15.4), 38.2 (d, C(5), 3 Jpccc=13.5), 15.9 (d, PCH 3 , Jpc=99.05). 20 (S)-(4-Aminocyclopent-1-enyl)methylphosphinic acid 1 H NMR (D 2 0): 8 7.51 (in, 2H), 6.11 (d, 1H, J=9.8), 3.96 (in, 1H), 2.86 (in, 2H), 2.46 (in, 2H), 1.22 (d, 3H, J=14.1); 13 C-NMR (D 2 0): 8 136.8 (d, C(2), 2 JpCc=11.5), 135.56 (d, C (1), Jpc=118.0), 51.0 (d, C(4), 3 Jpccc=l0.3), 38.9 (d, C(3), 2 Jpcc=15.4), 38.2 (d, C(5), 3 Jpccc=13.5), 15.9 (d, PCH 3 , Jpc=99.05). 25 (R)-(4-Aminocyclopent-1-enyl)methylphosphinic acid 1 H NMR (D 2 0): 6 7.51 (in, 2H), 6.11 (d, 1H, J=9.8), 3.96 (in, 1H), 2.86 (in, 2H), 2.46 (in, 2H), 1.22 (d, 3H, J=14.1); 13 C-NMR (D 2 0): 6 136.8 (d, C(2), 2 Jpcc=l1.5), 135.56 (d, C (1), Jpc=118.0), 51.0 (d, C(4), 3 Jpccc=l0.3), 38.9 (d, C(3), 2 Jpcc=15.4), 38.2 (d, 3 0 C(5), 3 Jpccc=13.5), 15.9 (d, PCH 3 , JPC= 9 9 .05).

WO 2006/000043 PCT/AU2005/000928 - 32 A similar procedure was used to prepare compounds (16) to (19). The characteristics of these compounds, as well as the enantiopure phosphinic amino acids corresponding to compound (18), are described below. 5 (±)-(4-Aminocyclopent-1-enyl)ethylphosphinic acid (16) 1H NMR (D 2 0): 6 6.17 (bd, 1, J=9.2), 6.17 (bd, 1, J=9.2), 3.95 (bsept, 1), 2.86 (bdd, 2, J=7.4, 16.5), 2.46 (bd, 2, J=18.1), 1.63 (dsept, 1, J=12.15), 1.48 (m, 2), 0.81(t, 3, J=6.9). ( )-(4-Aminocyclopent-1-enyl)isopropylphosphinic acid (17) 10 1 H NMR (D 2 0): 6 7.55 (m, 2H), 6.17 (dm, 1H, J=9.1), 3.95 (m, 1H), 2.86 (dd, 2H, J=7.5, J=16.8), 2.47 (d, 2H, J=16.2), 1.63 (m, 1H), 0.94 (t, 3H, J=7.1), 0.88 (t, 3H, J=7.2); "C NMR (D 2 0): 6 138.87 (d, C (2), 2 Jpcc=9.3), 137.56 (d, C (1), JPc=120.0), 50.98 (d, C (4), 3 Jpecc=9.4), 38.98 (apparent t, C (3) and C (5), 3 Jpcc=13.8), 27.84 (d, PCH (CH 3

)

2 , JPC101 -1), 15.19 (dd, PCH (CH 3

)

2 , J=2.3, J=27.0). 15 (±)-(4-Aminocyclopent-1-enyl)butylphosphinic acid (18) 1H NMR (D 2 0): 6 7.54 (m, 2H), 6.12 (dm, 1H, J=9.2), 3.95 (m, 1H) 2.85 (dd, 2H, J=7.7, J=16.1), 2.46 (dd, 2H, J=3.4, J=18.2), 1.47 (m, 2H), 1.27 (m, 4H), 0.76 (t, 1H, J=7.1); 1 3 C NMR (D 2 0): 6 137.68 (d, C (2), 2 Jpcc=10.2), 132.23 (d, C (1), Jpc=121.

8 ), 20 50.94 (d, C (4), J=10.1), 38.90 (d, C (3), 3 Jpccc=14.8), 38.53 (d, C (5), 2 Jpcc=l2.9), 29.61 (d, PCH 2

(CH

2

)

2

CH

3 , J=98.7), 24.24 (d, P (CH 2

)

2

CH

2

CH

3 , 3 Jpccc=3.6), 23.74 (d,

PCH

2

CH

2

CH

2

CH

3 , 2jrCc=1 6 .1), 13.15 (s, P (CH2)3CH3). (S)-(4-Aminocyclopent-1-enyl)butylphosphinic acid 25 1H NMR (D 2 0): 6 7.54 (m, 2H), 6.12 (dm, 1H, J=9.2), 3.95 (m, 1H) 2.85 (dd, 2H, J=7.7, J=16.1), 2.46 (dd, 2H, J=3.4, J=18.2), 1.47 (m, 2H), 1.27 (m, 4H), 0.76 (t, 1H, J=7.1); "C NMR (D 2 0): 6 137.68 (d, C (2), 2 JpcC=10.2), 132.23 (d, C (1), Jrc=121.

8 ), 50.94 (d, C (4), J=10.1), 38.90 (d, C (3), 3 Jpccc=l4.8), 38.53 (d, C (5), 2 jPcc=12.9), 29.61 (d, PCH 2

(CH

2

)

2

CH

3 , J=98.7), 24.24 (d, P (CH 2

)

2

CH

2

CH

3 , 3 Jpccc=3.6), 23.74 (d, 30 PCH 2

CH

2

CH

2

CH

3 , 2 Jcc=l6.1), 13.15 (s, P (CH 2

)

3

CH

3 ). (R)-(4-Aminocyclopent-1-enyl)butylphosphinic acid 1 H NMR (D 2 0): 6 7.54 (m, 2H), 6.12 (dm, 1H, J=9.2), 3.95 (m, 1H) 2.85 (dd, 2H, J=7.7, J=16.1), 2.46 (dd, 2H, J=3.4, J=18.2), 1.47 (m, 2H), 1.27 (m, 4H), 0.76 (t, 1H, WO 2006/000043 PCT/AU2005/000928 - 33 J=7.1); 1 3 C NMR (D 2 0): 8 137.68 (d, C (2), 2 Jpcc=10.2), 132.23 (d, C (1), Jpc=121.8), 50.94 (d, C (4), J=10.1), 38.90 (d, C (3), 3Jpccc=14.8), 38.53 (d, C (5), 2Jcc=12.9), 29.61 (d, PCH 2

(CH

2

)

2

CH

3 , J=98.7), 24.24 (d, P (CH 2

)

2

CH

2

CH

3 , 3 Jpccc=3.6), 23.74 (d,

PCH

2

CH

2

CH

2

CH

3 , 2 Jpcc=16.1), 13.15 (s, P (CH 2

)

3

CH

3 ). 5 ( )-(4-Aminocyclopent-1-enyl)benzylphosphinic acid (19) 1 H NMR (D 2 0): 6 7.1-7.6 (in, 6), 6.07 (bd, 1, J=9.2), 3.88 (in, 1), 2.73 (bdd, 2, J=5.0, J=38.2), 2.38 (bt, 2, J=19.0). 10 Example 2 - Electrophysiology The activity of compounds (15), (16), (17), (18) and (19) on GABA receptor sub-types were determined as described in Chebib, M., Mewett, K.N., Johnston, G.A.R., 1998, 15 "GABAc receptor antagonists differentiate between human pl and p2 receptors expressed in Xenopus oocytes", European Journal ofPharmacology 357, 227-234. The results are set out in Table 1. In this method, oocytes were harvested from Xenopus laevis and defolliculated. The 20 oocytes were then stored in ND96 solution (96 mM NaCl, 2 mM KCl, 1.8 mM CaC1 2 .2H 2 0, 1 mM MgCl 2 .6H 2 0, 5 mM HEPES (hemi-Na), pH 7.5) supplemented with 2.5 mM\4 sodium pyruvate, 0.5 mM theophylline and 50 pgml 1 gentamycin. The storage solution was changed daily. 25 Stage V-VI oocytes were injected with mRNA (10 ng / 50 nl) and then stored at 16"C. Recordings of receptor activity were obtained after two to eight days by a two-electrode voltage clamp by means of a Geneclamp 500 amplifier (Axon Instruments Inc., Foster City, CA), a MacLab 2e recorder (AD Instruments, Sydney, NSW) and Chart version 3.6.3 program. Oocytes were voltage clamped at -60 mV and the preparation was 30 continually perfused with ND96 solution at room temperature. Known concentrations of agonists and antagonists dissolved in ND96 were applied in the absence and presence of GABA respectively until maximum current was reached, at which time the oocyte was washed for five to ten minutes to allow complete recovery of response to a known dose WO 2006/000043 PCT/AU2005/000928 - 34 of GABA. In the case of antagonists, two dose response curves were conducted on the same cell to enable calculation of single point estimates: a GABA dose-response curve and a GABA dose-response curve in the presence of a known concentration of antagonist. All compounds were tested on oocytes from at least three harvests. 5 Table 1: Activity of Compounds on GABA receptor subtypes Compound GABAA GABAB (GB 1) GABAc (p1) Selectivity (a l p2y2L) 15 Antagonist Partial Agonist Antagonist GABAc

(IC

5 o > 300pM) (EC 5 0 = 44.62 p.M (IC 5 0 = 0.85p.M ~50x 0.23pM) 0.23p.M) 16 Antagonist Antagonist Antagonist GABAc

(IC

50 > 600pM) (IC 5 o > 300pM) (IC 50 = 12.32 p.M ~25x ± 3.97p.M) 17 Antagonist Antagonist Antagonist GABAc

(IC

5 0 > 600pM) (IC 50 > 300pM) (IC 50 = 6.34 ~50x 2.12p.M) 18 Antagonist Antagonist Antagonist GABAc

(IC

5 o > 300pM) (IC 50 ~ 300pM) (IC 50 = 3.68pM -100x 0.67pM) 19 Antagonist (No effect ~ 30p.M) Antagonist

(IC

50 > 300p.M) The results set out in Table 1 demonstrate that the compounds of the present invention 10 are highly selective GABAc receptor antagonists. The compounds of the present invention are much more selective GABAc receptor antagonists than compound (19). Example 3 - Comparison with ()-(3-aminocyclopent-1-enyl)methylphosphinic acid 15 (±)-(3-Aminocyclopent-1-enyl)methylphosphinic acid was prepared as described below. This compound is similar to compound (15) referred to above, but the amino group is at WO 2006/000043 PCT/AU2005/000928 - 35 the 3-position of the pentene ring rather than the 4-position. (±)-Ethyl(3-aminocyclopentenyl)methylphosphinate was prepared as described in WO 03/045897 and was dissolved in aqueous HCl (6M, 40 ml) and the solution heated 5 to reflux for 30 h. After cooling, the solution was evaporated to dryness under reduced pressure. The residue was dissolved in water (10 ml) and applied to an ion exchange column (Dowex 50, H* form). The column was washed with water until the washings were colourless and pH neutral and then eluted with aqueous pyridine (1M). Ninhydrin positive fractions were combined and evaporated to dryness under reduced pressure. 10 Residual traces of pyridine were removed by repeatedly redissolving the compound in water (20 ml) and re-evaporating (3 times). Recrystallisation from ethanol/acetone and drying gave (h)-(3-aminocyclopent-1-enyl)methylphosphinic acid. The activity of this compound on the GABA receptor sub-types was determined by the 15 same procedure as described in Example 2 for compounds (15) to (19). (±)-3 Aminocyclopente-l-nyl)methylphosphinic acid (200 tM) had no effect alone on p1 GABAc receptors but in the presence of 1 ptM GABA inhibited the response by 65%. The compound is therefore 50-100 times less active at GABAc than compound (15). 20 As can be seen from these results, compound (15) of the present invention is a much more active GABAc receptor antagonist than (±)-(3-aminocyclopent- 1 -enyl)methyl phosphinic acid. This result demonstrates that the position of the double bond in the cyclopentene ring greatly effects the selectivity of the compounds of the present invention. 25 The compounds of the present invention are selective GABAc receptor antagonists, and can therefore be used to enhance the cognitive activity of animals, including humans. The ability of the compounds of the present invention to enhance cognitive activity in 30 an animal can be demonstrated by tests known in the art, such as the Morris Water Maze test and the day-old chick model of memory (Gibbs & Ng 1977; Gibbs & Summers, 2002). Such tests can also be used to determine effective dosages of a selective GABAc receptor antagonist for enhancing the cognitive activity of an animal, and as an animal model for determining suitable effective dosages for humans. 35 It will be apparent to the person skilled in the art that while the invention has been described in some detail for the purposes of clarity and understanding, various WO 2006/000043 PCT/AU2005/000928 - 36 modifications and alterations to the embodiments described herein may be made without departing from the scope of the inventive concept disclosed in the specification. A reference herein to a prior art document is not an admission that the document forms 5 part of the common general knowledge in the art in Australia or in any other country. In the claims which follow and in the preceding description of the invention, except where the context requires otherwise due to express language or necessary implication, the word "comprising" is used in an inclusive sense, i.e. to specify the presence of the 10 stated features but not to preclude the presence or addition of further features in various embodiments of the invention.

WO 2006/000043 PCT/AU2005/000928 - 37 References Chebib M., Vandenberg R.J., Froestl W. and Johnston G.A.R. Eur. J Pharmacol., 1997 329, 223-229 5 Chebib M. Chemistry in Australia, October 2001, 19-21 Chebib M. and Johnston G.A.R. J. Med. Chem., 2000 43, 1427-1447 10 Drew C. A., Johnston G. A. R. and Weatherby R. P. Neurosci. Let. 1984 52, 317-321 Feigenspan A. W6ssle H. and Bormann J. Nature, 1993 361, 159-162 Froestl W., Mickel, S. J., von Sprecher, G., Diel. P. J., Hall, R. G., Maier, L., Strub, D., 15 Melillo, V., Baumann, P. A., Bernasconi, R., Gentsch, C., Hauser, K., Jaekel, J., Karlsson, G., Klebs, K., Maitre, L., Marescaux, C., Pozza, M. F., Schmutz, M., Steinmann, M. W., Riezen, H., Vassout, A., Mondadori, C., Olpe, H-R., Waldmeier, P.C., and Bittiger, H. J Med. Chem., 1995, 38, 3313-3331 20 Irwin, S. "Comprehensive Observational Assessment: l a. A Systematic, Quantitative Procedure for Assessing the Behavioural and Physiologic State of the Mouse", Psychopharmacologia, 1968 13, 222-257 Johnston, G.A.R., Curtis, D.R., Beart, P.M., Game, C.J.A., McCulloch, R.M. and 25 Twitchin, B. J. Neurochem., 1975 24, 157-160 Johnston, G.A.R., Allan, R.D., Kennedy, S.M.E. and Twitchin, B. "GABA Neurotransmitters", Alfred Benzon Symposium 12, Munksgaard, 1978, p 149-164. 30 Johnston, G.A.R. Pharmacol. Other , 1996 69, 173-198 ("Johnston, 1996a") Johnston, G.A.R. Trends Pharmacol. Sci., 1996 17, 319-323 ("Johnston, 1996b") Kerr, D.I.B. and Ong, J. Pharmacol. Ther., 1995 67, 187-246 35 Murata, Y., Woodward, R.M., Miledi, R. and Overman, L.E. Bioorg. and Med. Chem. Lett., 1996 6, 2071-2076 WO 2006/000043 PCT/AU2005/000928 - 38 Piers, E., Grierson, J.R., Lau, C.K. and Nagakura, I. Can. J. Chem. 1982, 60, 210 Qian, H. and Dowling, J.E. Nature, 1993 361, 162-164 5 Ragozzino, D., Woodward, R.M., Murata, F., Eusebi, F., Overman, L.E. and Miledi, R. Mol. Pharmacol., 1996 5(L 1024-1030 Woodward, R.M., Polenzani, L. and Miledi, R. Mol. Pharmacol., 1993 43, 609-625 10 Chebib M., Vandenberg R.J., Froestl W. and Johnston G.A.R. Eur. J Pharmacol., 1997 329, 223-229 Chebib M. Chemisty in Australia, October 2001, 19-21 15 Chebib M. and Johnston G.A.R. J Med. Chem., 2000 43, 1427-1447 Drew C. A., Johnston G. A. R. and Weatherby R. P. Neurosci. Let. 1984 52, 317-321 20 Feigenspan A. Wbssle H. and Bormann J. Nature, 1993 361, 159-162 Froestl W., Mickel, S. J., von Sprecher, G., Diel. P. J., Hall, R. G., Maier, L., Strub, D., Melillo, V., Baumann, P. A., Bernasconi, R., Gentsch, C., Hauser, K., Jaekel, J., Karlsson, G., Klebs, K., Maitre, L., Marescaux, C., Pozza, M. F., Schmutz, M., 25 Steinmann, M. W., Riezen, H., Vassout, A., Mondadori, C., Olpe, H-R., Waldmeier, P.C., and Bittiger, H. J. Med. Chem., 1995, 38, 3313-3331 Gibbs, M. E. and Ng, K. T., 1977. Psychobiology of memory: towards a model of memory formation. Biobehav. Reviews, 1, 113-136. 30 Gibbs, M. E. and Summers, R. J., 2002. Role of adrenoceptor subtypes in memory consolidation. Prog Neurobiol., 67, 345-391 Irwin, S. "Comprehensive Observational Assessment: 1 a. A Systematic, Quantitative 35 Procedure for Assessing the Behavioural and Physiologic State of the Mouse", Psychopharmacologia, 1968 13, 222-257 WO 2006/000043 PCT/AU2005/000928 - 39 Johnston, G.A.R., Curtis, D.R., Beart, P.M., Game, C.J.A., McCulloch, R.M. and Twitchin, B. J. Neurochem., 1975 24, 157-160 Johnston, G.A.R., Allan, R.D., Kennedy, S.M.E. and Twitchin, B. "GABA 5 Neurotransmitters", Alfred Benzon Symposium 12, Munksgaard, 1978, p 149-164 Johnston, G.A.R. Pharmacol. Ther., 1996 69, 173-198 ("Johnston, 1996a") Johnston, G.A.R. Trends Pharmacol. Sci., 1996 17, 319-323 ("Johnston, 1996b") 10 Kerr, D.I.B. and Ong, J. Pharmacol. Ther., 1995 67, 187-246 Murata, Y., Woodward, R.M., Miledi, R. and Overman, L.E. Bioorg. and Med. Chem. Lett., 1996 6, 2071-2076 15 Piers, E., Grierson, J.R., Lau, C.K. and Nagakura, I. Can. J Chemn. 1982, 60, 210 Qian, H. and Dowling, J.E. Nature, 1993 361, 162-164 20 Ragozzino, D., Woodward, R.M., Murata, F., Eusebi, F., Overman, L.E. and Miledi, R. Mol. Pharmacol., 1996 50 1024-1030 Woodward, R.M., Polenzani, L. and Miledi, R. Mol. Pharmacol., 1993 43, 609-625

Claims (11)

1. A compound of the formula I: 0 R // HO 5 wherein R is methyl, ethyl, propyl, isopropyl, butyl, pentyl, neo-pentyl or 10 cyclohexyl, or a salt or solvate thereof.

2. A method of selectively antagonising GABAc receptors compared to GABAB or GABAA receptors, comprising the step of exposing the receptors to an effective amount of a compound of formula I as defined in claim 1 or a 15 pharmaceutically acceptable salt or solvate thereof.

3. A method of enhancing the cognitive activity of an animal, comprising the step of administering to the animal an effective amount of a compound of formula I as defined in claim 1 or a pharmaceutically acceptable salt or solvate thereof. 20

4. A method of stimulating memory capacity in an animal, comprising the step of administering to the animal an effective amount of a compound of formula I as defined in claim 1 or a pharmaceutically acceptable salt or solvate thereof. 25

5. A method according to claim 3 or 4 wherein the animal is suffering from one or more conditions selected from the group consisting of cognitive deficit, memory impairment and dementia.

6. A method according to any one of claims 3 to 5 wherein the animal is suffering 30 from dementia, Alzheimer's disease, AIDS or schizophrenia.

7. A method according to any one of claims 3 to 6 wherein the animal is a human. WO 2006/000043 PCT/AU2005/000928 - 41

8. Use of a compound of formula I as defined in claim 1 or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for selectively antagonising GABAc receptors compared with GABAB or GABAA receptors. 5

9. Use of a compound of formula I as defined in claim 1 or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for enhancing the cognitive activity of an animal.

10 10. Use of a compound of formula I as defined in claim 1 or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for stimulating memory capacity in an animal.

11. A pharmaceutical composition comprising a compound of formula I as defined 15 in claim 1 or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable carrier.