GB921533A - Cyclopentanophenanthrene derivatives and process for the production thereof - Google Patents
Cyclopentanophenanthrene derivatives and process for the production thereofInfo
- Publication number
- GB921533A GB921533A GB2382559A GB2382559A GB921533A GB 921533 A GB921533 A GB 921533A GB 2382559 A GB2382559 A GB 2382559A GB 2382559 A GB2382559 A GB 2382559A GB 921533 A GB921533 A GB 921533A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- double bond
- keto
- hydroxy
- compounds
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J75/00—Processes for the preparation of steroids in general
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises compounds of the formula:- <FORM:0921533/IV(a)/1> wherein A is a single or a double bond between C1 and C2; X is F, Cl, or Br; Y is b -hydroxy or keto; R is hydrogen or an optionally substituted hydrocarbon carboxylic acid acyl group of less than 12 carbon atoms; and their preparation by subjecting 6a ,16a -dimethyl-D 4-pregnene-17a ,21-diol-3,20-dione to a fermentative oxygenation with Rhizopus nigricans or Aspergillus niger to introduce an 11a -hydroxyl group and transforming the ensuing triol by dehydration at C9-C11, addition of the elements of hypobromous acid to the resulting double bond, epoxide ring closure, ring opening with HF or HCl and optionally oxidation of the 11b -hydroxy group to an 11-keto group and/or esterification and/or dehydrogenation with SeO2 to form the corresponding D 1 compounds. Specification 921,534 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MX5155158 | 1958-07-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB921533A true GB921533A (en) | 1963-03-20 |
Family
ID=19742857
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2382559A Expired GB921533A (en) | 1958-07-12 | 1959-07-10 | Cyclopentanophenanthrene derivatives and process for the production thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB921533A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0110041A1 (en) * | 1982-11-22 | 1984-06-13 | Schering Aktiengesellschaft | 6-Alpha-methyl-corticoids, their preparation and utilization |
-
1959
- 1959-07-10 GB GB2382559A patent/GB921533A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0110041A1 (en) * | 1982-11-22 | 1984-06-13 | Schering Aktiengesellschaft | 6-Alpha-methyl-corticoids, their preparation and utilization |
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