WO2005068478A1 - Process for the production of asymmetric transformation catalysts - Google Patents

Process for the production of asymmetric transformation catalysts Download PDF

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Publication number
WO2005068478A1
WO2005068478A1 PCT/GB2005/000125 GB2005000125W WO2005068478A1 WO 2005068478 A1 WO2005068478 A1 WO 2005068478A1 GB 2005000125 W GB2005000125 W GB 2005000125W WO 2005068478 A1 WO2005068478 A1 WO 2005068478A1
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substituted
unsubstituted
mmol
room temperature
nmr
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French (fr)
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Wei-Ping Chen
John Whittall
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Phoenix Chemicals Ltd
Stylacats Ltd
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Phoenix Chemicals Ltd
Stylacats Ltd
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Priority to CA002553608A priority Critical patent/CA2553608A1/en
Priority to US10/586,204 priority patent/US20080281106A1/en
Priority to EP05701893A priority patent/EP1725570B1/en
Priority to AU2005205229A priority patent/AU2005205229B2/en
Priority to DE602005008917T priority patent/DE602005008917D1/de
Priority to JP2006548403A priority patent/JP2007517850A/ja
Publication of WO2005068478A1 publication Critical patent/WO2005068478A1/en
Anticipated expiration legal-status Critical
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    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
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    • B01J31/185—Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
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    • B01J31/1875—Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
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    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2447—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring
    • B01J31/2452—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom
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    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
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    • B01J31/2447—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring
    • B01J31/2452—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom
    • B01J31/2457—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom comprising aliphatic or saturated rings, e.g. Xantphos
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    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2495—Ligands comprising a phosphine-P atom and one or more further complexing phosphorus atoms covered by groups B01J31/1845 - B01J31/1885, e.g. phosphine/phosphinate or phospholyl/phosphonate ligands
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/48—Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof
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    • B01J2531/0202—Polynuclearity
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Definitions

  • This invention relates to a novel process for the production of asymmetric transformation catalysts, in particular to such a process for the production of phosphine and arsine ligands having a chiral centre at phosphorus, or arsenic as the case may be.
  • ligands are found to be useful in a wide variety of asymmetric transformation reactions, including hydrogenation and carbon- oxygen and carbon-nitrogen bond formation reactions.
  • the process of the invention may be applicable to the production of chiral catalysts containing aromatic ring systems generally, and is especially useful in the production of metallocene-based phosphine and arsine ligands.
  • the invention also relates to chiral catalysts produced by the process of the invention, and to the use of such catalysts in asymmetric transformation reactions.
  • Ppfa as well as bppfa and bppfoh proved to be effective ligands for the catalysis of a variety of asymmetric transformations. From this starting point, many chiral ferrocene-based bisphosphine ligands with a range of structural variation have been developed in the last few years.
  • Josiphos-type ligands are in widespread commercial use, having been found effective for Rh-catalyzed hydrogenation of ⁇ -acetamidocinnamate, dimethyl itaconate, and ⁇ -ketoesters. Because the two phosphine groups are introduced into the ligand in consecutive steps with high yields, a variety of ligands are available with widely differing steric and electronic properties. The ligands have already been applied in three production processes 3 , several pilot processes and many other syntheses.
  • PPF-tBu2 a Josiphos type ligand with a di-(tert-butyl)phosphino group
  • XyliPhos is another notable example.
  • Bophoz 6 is a combination of a phosphine and an aminophosphine and is prepared in 3 steps from ppfa with high overall yields.
  • the ligand is air stable and effective for the hydrogenation of enamides, itaconates and ⁇ -keto acid derivatives. As observed for several ligands forming seven-membered chelates, high activities can be reached and TONs up to 10,000 have been claimed. The full scope of this modular ligand class has not yet been explored.
  • Taniaphos A class of non-C 2 -symmetrical, ferrocene-based 1 ,5-diphosphine ligands, Taniaphos, has been developed by Knochel 7,8 . Compared to the Josiphos ligands, Taniaphos has an additional phenyl ring inserted at the side chain of the Ugi amine. Taniaphos gave excellent results in Rh- and Ru-catalyzed asymmetric hydrogenation. The configuration of ⁇ -position of Taniaphos plays an important role in the enantioselectivities and activities. The Taniaphos 1b with ⁇ S configuration leads to higher enantioselectivities and activities than 1a with ⁇ R configuration in a wide range of asymmetric transformations.
  • the TRAP ligands developed by Ito 11 form 9-membered metallocycles. However, it is not clear whether the cis-isomer, present in small amounts, or the major trans-isomer is responsible for the catalytic activity. Up to now only a few different PR2 fragments have been tested, but it is clear that the choice of R strongly affects the catalytic performance.
  • the Rh complexes work best at very low pressures of 0.5 + 1 bar and effectively reduces indole-derivatives, enamides and itaconic acid derivatives.
  • Kang 12 reported the C 2 -symmetry FerroPHOS with only planar chirality. FerroPHOS ligands are air-stable and are very efficient for the asymmetric hydrogenation of various dehydroamino acid derivitives (up to 99% ee).
  • JAFAPhos Another C 2 -symmetry planar chiral diphosphine, JAFAPhos, has been developed by Jendralla 13 . JAFAPhos gave excellent results in asymmetric hydrogenation, allylic alkylation, Grignard cross coupling and aldol reactions.
  • Kagan 14 reported plane chiral ferrocene-based bisphosphorus ligands 2 and 3, and up to 95% ee's have been obtained in asymmetric hydrogenation of dimethyl itaconate using these ligands as catalyst.
  • Another class of known diphosphine ligands exhibit chirality only at the phosphorus atoms:
  • FerroTANE chiral 1,1'-bis(phosphetano) ferrocenes
  • Mezzetti 18 and van Leeuwen 19 have independently reported P-chiral ferrocenyl bisphosphines 4a and 4b. These two ligands have shown excellent enantioselectivities (up to 99% ee) for asymmetric hydrogenation of ⁇ - dehydroamino acid derivatives.
  • Zhang has reported a 1,1'-bis(Phospholanyl) ferrocene ligand 5 with ketal substitutes at the 3 and 4 positions.
  • the ligand has shown excellent enantioselectivities in hydrogenation of ⁇ -dehydroamino acid derivatives.
  • the ketal groups of the ligand are important for achieving the high enantioselectivity, since the corresponding ligand without ketal groups only provides moderate ee's.
  • Zhang has also developed a 1,1'-bis(dinaphthophosphepinyl) ferrocene ligand, f-binaphane, which has been successfully applied in the Ir-catalyzed hydrogenation of acyclic aryl imines. 21
  • Reetz has developed a binaphthol-derived ferrocene-based bisphosphonite ligand 6 22 , which has shown excellent reactivities and enantioselectivities in Rh- catalyzed hydrogenation of itaconates and ⁇ -dehydroamino acid derivatives.
  • Another class of known ligands exhibits both planar and phosphorus chirality:
  • Van Leeuwen has reported ferrocene-based bisphosphines combining planar and phosphorus chirality 7a and 7b 23 . These two ligands have shown excellent enantioselectivities (up to 99% ee) for asymmetric allylic alkylations. Thus, most of the known ferrocene-based diphosphines contain planar and carbon chirality, only planar chirality or only phosphorus chirality. More recently, Togni reported the first tridentate ferrocene-based phosphine ligand 12 combining planar, phosphorus and carbon chirality. 24
  • R 1"5 , W, Q, n, m and G are variously defined, and a process for making such ligands.
  • the process described therein is found to be more generally applicable to the production of various chiral ligands.
  • a process for the production of chiral ligands comprising providing a starting material of Formula
  • X* is a chiral or achiral directing group
  • ⁇ is an optionally substituted mono- or polycyclic aryl or cycloalkyl group; ortholithiating the substrate; converting the ortho-lithiated substrate to a phosphine group having the formula -PR 1 R 1 , R 1 and R 1 being different from each other and independently selected from substituted and unsubstituted, branched- and straight-chain alkyl, alkoxy, alkylamino, substituted and unsubstituted cycloalkyl, substituted and unsubstituted cycloalkoxy, substituted and unsubstituted cycloalkylamino, substituted and unsubstituted carbocyclic aryl, substituted and unsubstituted carbocyclic aryloxy, substituted and unsubstituted heteroaryl, substituted and unsubstituted heteroaryloxy, substituted and unsubstituted carbocyclic arylamino and substituted and unsubstituted heteroarylamino,
  • ⁇ is, in one such process according to the invention, one aromatic ring (optionally further substituted) of a metallocene compound.
  • a process for the production of chiral ligands comprising providing a starting material of Formula (A): (A ) wherein X* is a chiral or achiral directing group; and
  • ⁇ is an optionally substituted mono- or polycyclic aryl or cycloalkyl group; ortholithiating the substrate; reacting the ortholithiated substrate with an R 1 substituted phosphine or arsine, R 1 being selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen; and then with an R 1 -bearing Grignard reagent or organolithium compound, R 1 being different from R 1 and being selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl
  • R >1-5 , W, Q, n, m and G are as defined in GB0400720.9.
  • O is, in one such process according to the invention, one aromatic ring (optionally further substituted) of a metallocene compound.
  • the process of the invention may be used in the production of phosphine or arsine ligands having up to three elements of chirality; planar chirality, chirality at phosphorus (or arsenic), and optionally chirality at carbon.
  • the invention further provides chiral ligands obtained by the process of the invention.
  • ligands include metallocene-based phosphine ligands having planar, phosphorus and carbon chirality.
  • the invention further provides chiral ligands (other than those of Formula (I), (II) or (III)) obtained by the process of the invention.
  • chiral ligands include metallocene-based phosphine ligands having planar, phosphorus and carbon chirality.
  • Ligands obtained by a process according to the invention have particular advantages over prior art ligands because the provision of up to three chiralities allows the designer of a ligand greater scope than has hitherto been the case to design ligands for a particular purpose.
  • the introduction of phosphorus chirality may enhance the chiral discrimination produced by the catalyst when a matching among the planar chirality, carbon chirality and the chirality of phosphorus can be achieved.
  • a matching catalyst may give high ee and a mismatching one may give low ee.
  • transition metal complex containing transition metal coordinated to the ligand produced by the process of the invention.
  • the metal is preferably a Group Vlb or a Group VIII metal.
  • X* is an ortho directing group.
  • Synthesis of phosphorus chiral phosphines may be effected in accordance with the invention with the use of a suitable chiral onffto-directing group, for example in accordance with the following scheme: 1) n-BuLi or
  • R 1 Z is an organoal ali species or Grignard reagent
  • R, R 2 and R 3 are independently selected from substituted and , unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen.
  • synthesis of ferrocene-based phosphorus chiral phosphines may be effected with the use of a suitable chiral otf ⁇ o-directing group, for example in accordance with the following schemes:
  • L is a linker.
  • L may be selected from ferrocene, diphenyl ethers, xanthenes, 2,3-benzothiophene, 1,2-benzene, succinimides and many others.
  • dianionic linkers may be made from a corresponding di-halo precursor, eg:
  • dianionic linkers may be represented as follows:
  • ferrocene is a preferred linker in accordance with the invention.
  • the invention provides a method for preparing a phosphine ligand chiral at phosphorus comprising providing an optionally substituted mono- or polyaromatic or cycloalkyl substrate having a chiral or achiral directing substituent on at least one ring, and subjecting the substrate to an ortho- lithiation step before subsequently converting the ortho-lithiated substrate to a phosphine group having the formula -PR 1 R 1 " or PR 1 L, wherein L is a linker as previously defined and wherein, R 1 and R 1 are different from each other and are independently selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen, and optionally or if necessary converting the directing substitu
  • the invention provides a method for preparing a phosphine ligand chiral at phosphorus comprising providing a metallocene-based substrate having a chiral or achiral directing substituent on at least one ring, and subjecting the substituted metallocene to an ortho-lithiation step before subsequently converting the ortho-lithiated substrate to a phosphine group having the formula -PR 1 R 1 " or PR 1 L, wherein L is a linker as previously defined and wherein, R 1 and R " are different from each other and are independently selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen, and optionally or if necessary converting the directing substituent to a chiral
  • the invention also provides a method for preparing an arsine ligand chiral at arsenic comprising providing an optionally substituted mono- or polyaromatic or cycloalkyl substrate having a chiral or achiral directing substituent on at least one ring, and subjecting the substrate to an ortho-lithiation step before subsequently converting the ortho-lithiated substrate to an arsine group having the formula -AsR 1 R 1 " or AsR 1 L, wherein L is a linker as previously defined and wherein, R 1 and R are different from each other and are independently selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen, and optionally or if necessary converting the directing substituent to a
  • the invention also provides a method for preparing an arsine ligand chiral at arsenic comprising providing a metallocene-based substrate having a chiral or achiral directing substituent on at least one ring, and subjecting the substituted metallocene to an ortho-lithiation step before subsequently converting the ortho- lithiated substrate to an arsine group having the formula -AsR 1 R 1 " or AsR 1 L, wherein L is a linker as previously defined and wherein, R 1 and R 1 are independently selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen, and optionally or if necessary converting the directing substituent to a chiral group, or to a different
  • one such method comprises providing a substrate of the Formula (A):
  • ⁇ is, in one such process according to the invention, one aromatic ring (optionally further substituted) of a metallocene compound.
  • Another method comprises providing a compound of the Formula (A): (A) wherein is an optionally substituted mono- or polycyclic aryl or cycloalkyl group;
  • X* is chiral directing group, and is preferably selected from the group as previously defined; ortholithiating the substrate; reacting the ortholithiated substrate with an R 1 substituted halophosphine or haloarsine, R 1 being selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen; and then with an R 1 -bearing Grignard reagent or organoalkali (preferably organolithium) compound, R 1' being selected from substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstit
  • R 1 , W, Q, n, m and G are as defined in GB0400720.9.
  • O is, in one such process according to the invention, one aromatic ring (optionally further substituted) of a metallocene compound.
  • One particularly preferred X* group in each of the above methods is R NMe 2
  • the ortho-lithiation step is preferably a mono-ortho-lithiation step using n- butyllithium, sec-butyllithium or tert-butyllithium.
  • the resulting monolithium compound is preferably reacted in situ with a dichlorophosphine of the formula R 1 PCI 2 followed by reacting with an organometallic reagent of the formula R 1 " Z, wherein R 1 and R 1 are as defined above; Z is Li or MgY wherein Y is a halide.
  • the synthesis preferably proceeds by converting compound (C) to compound D, E, or F:
  • R d is an acyl group
  • R e is selected from hydrogen, substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen, and R 1 , R 1" are as previously defined; and then: reacting compound D with a secondary phosphine of the formula R 6 R 7 PH wherein R 6 and R 7 are the same or different, and are independently selected from substituted and unsubstituted, branched- and straight-chain alkyl, alkoxy, alkylamino, substituted and unsubstituted cycloalkyl, substituted and unsubstituted cycloalkoxy, substituted and unsubstituted cycloalkylamino, substituted and unsubstitute
  • R 9 is selected from hydrogen, halogen, OR 10 , SR 10 , NR 10 R 11 , substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen; wherein R 10 , R 1 are the same or different and are independently selected from hydrogen, substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen, n' is 0 to 4, and Z is MgY (
  • R 9 is as previously defined;
  • R 12 is selected from hydrogen, substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen; or (R 12 )2 is -(CH2)m- , n' is 0 to 4; and m' is 1 to 8, to obtain compounds L and M:
  • Compound H may be reacted with a halophosphine of the formula R 6 R 7 PY wherein R 6 , R 7 are, as previously defined, and Y is chlorine, bromine or iodine, to obtain compound Q:
  • compound H may be reacted with an acid derivative of the formula R 13 COY wherein R 13 is selected from hydrogen, substituted and unsubstituted, branched- and straight-chain alkyl, substituted and unsubstituted cycloalkyl, substituted and unsubstituted carbocyclic aryl, and substituted and unsubstituted heteroaryl wherein the or each heteroatom is independently selected from sulphur, nitrogen, and oxygen, and Y is a halide, a sulphate, an imidazole, R 13 COO- or hydrogen, to obtain compound R:
  • compound H may be reacted with an acid derivative of the formula YOC-R * -COY and YOC-R * *-COY wherein R*, R** and Y are, as previously defined, to obtain the compounds having Formulae U and V:
  • R 14 is selected from OR 10 , SR 19 , NHR 10 and NR 19 R 11 , wherein R 10 , R 1 are as previously defined.
  • Suitable Chiral diamines include:
  • the invention provides a method for preparing a chiral diphosphine
  • ligand comprising a metallocene-based substrate having an achiral directing substituent on one or both rings, and subjecting the substituted metallocene to an enantioselective ortho-lithiation step before subsequently converting the ortho-lithiated substrate to a phosphorus chiral phosphine.
  • auxiliary chiral compound such as the chiral diamine
  • ortholithiation step Whilst the use of an auxiliary chiral compound (such as the chiral diamine) in the ortholithiation step may be preferred in some circumstances, where direct synthesis of a chiral product (in enantiomeric excess) is desired, it is also possible to ortholithiate in the absence of such a chiral auxiliary, and then resolve the enantiomeric product mixture at the end of the synthesis.
  • one method according to the present invention for preparing chiral ligands comprises providing a substrate of the formula A*:
  • X** is an achiral directing group, and is preferably as previously defined; and subjecting the compound to enantioselective mono-ortho-lithiation using n-butyllithium or sec-butyllithium or tert- butyllithium in the presence of a homochiral tertiary amine, and reacting the resulting chiral monolithium compound in situ with a dichlorophosphine of the formula R 1 PCl2 followed by reacting with an organometallic reagent of the formula R 1 M, wherein R 1 and R 1 are as defined hereinabove; M is Li or MgX wherein X is a halide, to obtain phosphorus chiral compound having formula C*:
  • One method according to the invention for preparing a ferrocene-based chiral ligand comprises providing a compound of the Formula B*:
  • PhPCI 2 (746 uL, 5.5 mmoL) was added via a syringe
  • the mixture was warmed to room temperature and stirred for 1 h at room temperature, the mixture was cooled to - 78 °C again, and a suspension of o-AnLi [prepared from 2-bromoanisole (805 uL, 6.5 mmol) and 1.7 M t-BuLi (7.6 mL, 13 mmol) in Et 2 O (30 mL) at -78 °C] was added via a cannula, then the mixture was stirred overnight at -78 °C to room temperature.

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WO2006012046A3 (en) * 2004-06-25 2006-04-27 Eastman Chem Co Preparation of aminophosphines
JP2008024596A (ja) * 2006-07-18 2008-02-07 Toyohashi Univ Of Technology 光学活性２，６−ビスアミノメチルピリジン誘導体とその製造方法およびその使用
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WO2011080736A1 (en) 2009-12-29 2011-07-07 Mapi Pharma Hk Limited Intermediate compounds and processes for the preparation of tapentadol and related compounds
CN114560893A (zh) * 2022-03-16 2022-05-31 中国科学院上海有机化学研究所 平面手性茂金属化合物、其合成方法及应用

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JP6840480B2 (ja) * 2015-07-23 2021-03-10 エボニック オペレーションズ ゲーエムベーハー エチレン性不飽和化合物のアルコキシカルボニル化のための、フェロセン系化合物及びこれに基づくパラジウム触媒
PT3272759T (pt) * 2016-07-19 2019-07-17 Evonik Degussa Gmbh Ligandos de 1,1¿-bis(fosfino)ferroceno para a alcoxicarbonilação
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WO2006012045A1 (en) * 2004-06-25 2006-02-02 Eastman Chemical Company Phosphine-phosphoramidite compounds
WO2006012046A3 (en) * 2004-06-25 2006-04-27 Eastman Chem Co Preparation of aminophosphines
US7906669B2 (en) * 2005-01-14 2011-03-15 Solvias Ag Metallocene-based phosphorus chiral phosphines
JP2008024596A (ja) * 2006-07-18 2008-02-07 Toyohashi Univ Of Technology 光学活性２，６−ビスアミノメチルピリジン誘導体とその製造方法およびその使用
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CN114560893A (zh) * 2022-03-16 2022-05-31 中国科学院上海有机化学研究所 平面手性茂金属化合物、其合成方法及应用
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