IL43146A - The preparation of 2-(omega-carbalkoxyalkyl)-4(r)-hydroxy-cyclopentane-1,3-diones by fermentative enzyme action of ascomycetes - Google Patents

The preparation of 2-(omega-carbalkoxyalkyl)-4(r)-hydroxy-cyclopentane-1,3-diones by fermentative enzyme action of ascomycetes

Info

Publication number
IL43146A
IL43146A IL43146A IL4314673A IL43146A IL 43146 A IL43146 A IL 43146A IL 43146 A IL43146 A IL 43146A IL 4314673 A IL4314673 A IL 4314673A IL 43146 A IL43146 A IL 43146A
Authority
IL
Israel
Prior art keywords
cyclopentane
trione
hydroxy
microorganism
carbalkoxyalkyl
Prior art date
Application number
IL43146A
Other languages
English (en)
Other versions
IL43146A0 (en
Original Assignee
Wisconsin Alumni Res Found
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wisconsin Alumni Res Found filed Critical Wisconsin Alumni Res Found
Publication of IL43146A0 publication Critical patent/IL43146A0/xx
Publication of IL43146A publication Critical patent/IL43146A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P31/00—Preparation of compounds containing a five-membered ring having two side-chains in ortho position to each other, and having at least one oxygen atom directly bound to the ring in ortho position to one of the side-chains, one side-chain containing, not directly bound to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having at least one oxygen atom bound in gamma-position to the ring, e.g. prostaglandins
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C405/00—Compounds containing a five-membered ring having two side-chains in ortho position to each other, and having oxygen atoms directly attached to the ring in ortho position to one of the side-chains, one side-chain containing, not directly attached to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having oxygen atoms attached in gamma-position to the ring, e.g. prostaglandins ; Analogues or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
    • C07C69/716—Esters of keto-carboxylic acids or aldehydo-carboxylic acids
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/912—Absidia
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/913—Aspergillus
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/913—Aspergillus
    • Y10S435/919—Aspergillus ustus
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/93—Hansenula
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/931—Mucor
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/933—Penicillium
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/94—Saccharomyces
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/94—Saccharomyces
    • Y10S435/942—Saccharomyces cerevisiae
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/944—Torulopsis
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms using fungi
    • Y10S435/945—Trichoderma
IL43146A 1972-09-29 1973-09-03 The preparation of 2-(omega-carbalkoxyalkyl)-4(r)-hydroxy-cyclopentane-1,3-diones by fermentative enzyme action of ascomycetes IL43146A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US29345772A 1972-09-29 1972-09-29

Publications (2)

Publication Number Publication Date
IL43146A0 IL43146A0 (en) 1973-11-28
IL43146A true IL43146A (en) 1976-05-31

Family

ID=23129170

Family Applications (1)

Application Number Title Priority Date Filing Date
IL43146A IL43146A (en) 1972-09-29 1973-09-03 The preparation of 2-(omega-carbalkoxyalkyl)-4(r)-hydroxy-cyclopentane-1,3-diones by fermentative enzyme action of ascomycetes

Country Status (22)

Country Link
US (1) US3773622A (xx)
JP (1) JPS543953B2 (xx)
AR (1) AR198695A1 (xx)
AT (1) AT333689B (xx)
BE (1) BE805491A (xx)
BG (1) BG23209A3 (xx)
CA (1) CA997696A (xx)
CH (1) CH601143A5 (xx)
DD (1) DD107434A5 (xx)
ES (1) ES419174A1 (xx)
FR (1) FR2201276B1 (xx)
GB (1) GB1408732A (xx)
HU (1) HU168883B (xx)
IE (1) IE38191B1 (xx)
IL (1) IL43146A (xx)
NL (1) NL7312906A (xx)
NO (1) NO138334C (xx)
PH (1) PH10248A (xx)
PL (1) PL91090B1 (xx)
RO (6) RO63492A (xx)
SE (1) SE397085B (xx)
ZA (1) ZA735999B (xx)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3968141A (en) * 1972-11-27 1976-07-06 Wisconsin Alumni Research Foundation Processes for stereospecifically preparing chiral 2-substituted-4-hydroxy-2-cyclopenten-1-one
US4172953A (en) * 1973-03-30 1979-10-30 G. D. Searle & Co. 2,3,5-Trisubstituted cyclopentanealkenoic acids, derivatives thereof and intermediates thereto
US3925156A (en) * 1973-12-10 1975-12-09 Miles Lab Microbiological process for preparing 2-substituted-4-(r)-hydroxy-cyclopentane-1,3-diones
US4057851A (en) * 1974-06-12 1977-11-08 Wisconsin Alumni Research Foundation Chiral 2-substituted-4-hydroxy-2-cyclopenten-1-one
US4052434A (en) * 1974-08-21 1977-10-04 The Regents Of The University Of California Prostaglandin intermediates
GB1528382A (en) * 1974-12-26 1978-10-11 Teijin Ltd Cyclopentene diols and acyl esters thereof and processes for their preparation
US4159998A (en) * 1978-09-11 1979-07-03 Miles Laboratories, Inc. Process for the preparation of 2-(7-hydroxyalkyl)-4R, 4S or 4RS -hydroxy-cyclopent-2-enone

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR6915378D0 (pt) * 1969-08-22 1973-01-16 Syntex Corp Aperfeicoamento num processo para a preparacao de 1-beta hidroxi-3-oxo-ciclo-alcanos

Also Published As

Publication number Publication date
ATA839573A (de) 1976-04-15
DE2348471A1 (de) 1974-04-18
CA997696A (en) 1976-09-28
PL91090B1 (xx) 1977-02-28
RO63801A (fr) 1978-10-15
FR2201276B1 (xx) 1977-05-27
JPS4975786A (xx) 1974-07-22
BG23209A3 (xx) 1977-07-12
ZA735999B (en) 1974-09-25
IE38191L (en) 1974-03-29
IL43146A0 (en) 1973-11-28
RO63802A (fr) 1978-11-15
CH601143A5 (xx) 1978-06-30
RO63799A (fr) 1978-12-15
DE2348471B2 (de) 1975-08-28
AT333689B (de) 1976-12-10
RO63800A (fr) 1978-10-15
PH10248A (en) 1976-10-14
BE805491A (fr) 1974-01-16
NL7312906A (xx) 1974-04-02
ES419174A1 (es) 1976-04-16
AR198695A1 (es) 1974-07-15
JPS543953B2 (xx) 1979-02-28
NO138334B (no) 1978-05-08
SE397085B (sv) 1977-10-17
IE38191B1 (en) 1978-01-18
DD107434A5 (xx) 1974-08-05
RO63803A (fr) 1978-11-15
NO138334C (no) 1978-08-16
HU168883B (xx) 1976-07-28
GB1408732A (en) 1975-10-01
AU5991473A (en) 1975-03-06
FR2201276A1 (xx) 1974-04-26
US3773622A (en) 1973-11-20
RO63492A (fr) 1978-10-15

Similar Documents

Publication Publication Date Title
Inagaki et al. One-pot synthesis of optically active cyanohydrin acetates from aldehydes via lipase-catalyzed kinetic resolution coupled with in situ formation and racemization of cyanohydrins
Wang et al. Lipase-catalyzed irreversible transesterification using enol esters: resolution of cyanohydrins and syntheses of ethyl (R)-2-hydroxy-4-phenylbutyrate and (S)-propranolol
US4859784A (en) Process for the production of optically active cyanohydrins
Wong et al. Enzyme-catalyzed organic synthesis: regeneration of deuterated nicotinamide cofactors for use in large-scale enzymatic synthesis of deuterated substances
IL43146A (en) The preparation of 2-(omega-carbalkoxyalkyl)-4(r)-hydroxy-cyclopentane-1,3-diones by fermentative enzyme action of ascomycetes
Catterall et al. The configuration of the 1, 2-dihydroxy-1, 2-dihydronaphthalene formed in the bacterial metabolism of naphthalene
DK159327C (da) Fremgangsmaade til fremstilling af butanol ved gaering af carbonholdige forbindelser med clostridium acetobutylicum atcc 39236
Patterson et al. Enzymic conversion of. alpha.-keto aldehydes to optically active. alpha.-hydroxy acids using glyoxalase I and II
Takaishi et al. Bifunctional chiral synthons via microbiological methods. 2. optically-active α-hydroxy aldehydes.
EP0247620A2 (en) Production of cyclopentenones
JPH07507200A (ja) ピラノン
ATE19868T1 (de) Herstellung von natriumsalicylat.
Crestia et al. Transketolase and fructose-1, 6-bis-phosphate aldolase, complementary tools for access to new ulosonic acid analogues
Noma et al. Epimerization of (-)-isodihydrocarvone to (-)-dihydrocarvone by Pseudomonas fragi IFO 3458
Fadnavis et al. Biotransformations with baker's yeast: pH effects on diastereoselectivity during α-hydroxy-β-ketoester reductions and carbon carbon bond cleavages
US3616225A (en) Process for producing unsaturated steroids
GB1089920A (en) Process for preparing hydroxycycloalkanones
US3892630A (en) Process for preparing hydroxycyclopentenone derivatives using microorganisms
GB1379874A (en) Process for the preparation of cyclopentenes
Iguchi et al. Synthesis of clavulone derivatives. Selective cleavage of ester bonds in clavulone.
EP0783039B1 (en) Process for producing optically active 2-alkoxycyclohexanol derivatives
ES416971A1 (es) Procedimiento para la preparacion de derivados isoquinoli- na.
Gamalevich et al. A chemo-enzymatic approach to optically active 3-(4-methoxycarbonyl) phenyl-2-methyl-1-propanols
Kajiwara et al. Enzymatic formation of (2R)-hydroxy-and 2-oxo-hexadecanoic acid in Ulva pertusa and Porphyra sp.
US5374768A (en) Cyclohexene derivatives