McAleer et al., 1958 - Google Patents
Communications-1-Hydroxylation of 9α-FluorohydrocortisoneMcAleer et al., 1958
- Document ID
- 3556598885253264507
- Author
- McAleer W
- Kozlowski M
- Stoudt T
- Chemerda J
- Publication year
- Publication venue
- The Journal of Organic Chemistry
External Links
Snippet
Sir: Two reports of l-hydroxylation of steroids in-duced by microorganisms have appeared recently. The first1 relates to the production of la-hydroxy-4-androstene-3, 17-dione and 1 a- hydroxydehydroepiandrosterone with species of Penicillium and the second2 to the l£ …
- 238000005805 hydroxylation reaction 0 title abstract description 7
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0011—Androstane derivatives substituted in position 17 by a keto group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J13/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J7/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
- C07J7/0005—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21
- C07J7/001—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group
- C07J7/0015—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group not substituted in position 17 alfa
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes for the preparation of steroids in general
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0051—Estrane derivatives
- C07J1/0081—Substituted in position 17 alfa and 17 beta
- C07J1/0088—Substituted in position 17 alfa and 17 beta the substituent in position 17 alfa being an unsaturated hydrocarbon group
- C07J1/0096—Alkynyl derivatives
-
- 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—Micro-organisms
- Y10S435/911—Micro-organisms using fungi
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0036—Nitrogen-containing hetero ring
- C07J71/0042—Nitrogen only
-
- 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
- C12P33/00—Preparation of steroids
- C12P33/005—Degradation of the lateral chains at position 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4179336A (en) | Microbiological degradation of sterol side chains to a 17-keto group | |
US3684657A (en) | Selective microbiological degradation of steroidal 17-alkyls | |
Simpson et al. | Steroid biosynthesis in the testis of dogfish (Squalus acanthias) | |
McAleer et al. | Communications-1-Hydroxylation of 9α-Fluorohydrocortisone | |
Sih et al. | C22 acid intermediates in the microbiological cleavage of the cholesterol side chain | |
Eppstein et al. | Microbiological Transformations of Steroids. III. 1 Preparation of 11-Epi-corticosterone and of 6β-Hydroxy-11-desoxycorticosterone | |
Wechter et al. | 11-Oxygenated Pregnenolones. II. Synthesis of 11α-Hydroxy-, 11β-Hydroxy-, and 11-Ketopregnenolones and 11-Keto-17α-pregnenolone | |
Laskin et al. | Microbial hydroxylation of estrone and estradiol in the 6β-, 7α-, and 15α-positions | |
US2981659A (en) | Method for the microbiological conversion of pregnane series steroids | |
US2697715A (en) | Process for selective oxidation of 17beta-hydroxy group of 6beta-hydroxytestosterone | |
US2855410A (en) | 16 oxygenated steroidal compounds | |
US3067212A (en) | Production of equilin and intermediates | |
US3340278A (en) | 5(10), 7-estradiene-3, 17-dione and the process for the production thereof | |
Sax et al. | Microbiological 16-oxidation of Estr-4-en-3-one | |
IE44308B1 (en) | Process for the manufacture of 5-androsten-17-one derivatives and their use | |
Owen et al. | The biotransformation of hyodeoxycholic acid by Pseudomonas sp. NCIB 10590 under anaerobic conditions | |
US3117060A (en) | 16-methylene-testosterone derivatives | |
GB792803A (en) | Oxidation products from compounds of the steroid series and process of making same | |
US2787624A (en) | Process for converting delta4-3-keto-6-oxy pregnenes to delta4-3-keto pregnenes | |
NAMBARA et al. | Stereochemistry of Microbial Dehydrogenation of 5α-3-Ketosteroid | |
US3179674A (en) | 15-oxygenated estrones and estradiols | |
US3665022A (en) | Degradation of side chain in sapogenins | |
Madyastha et al. | Role of neutral metabolites in microbial conversion of 3β-acetoxy-19-hydroxycholest-5-ene into estrone | |
Mehdi et al. | Steroid biosynthesis by reptilian adrenals | |
US3578565A (en) | Process for the manufacture of steroids of the androstane series |