GB1104185A - Novel formyl-oestratrienes - Google Patents
Novel formyl-oestratrienesInfo
- Publication number
- GB1104185A GB1104185A GB22047/66A GB2204766A GB1104185A GB 1104185 A GB1104185 A GB 1104185A GB 22047/66 A GB22047/66 A GB 22047/66A GB 2204766 A GB2204766 A GB 2204766A GB 1104185 A GB1104185 A GB 1104185A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- formyl
- oestratrienes
- keto
- conventional methods
- 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
- QOTITYMKFHXGRE-IYHXRUFHSA-N 2-[(9R,10S,13S)-1,2,3,4,5,6,9,10,11,12-decahydrocyclopenta[a]phenanthren-13-yl]acetaldehyde Chemical class C(=O)C[C@@]12C=CC=C1C1=CCC3CCCC[C@@H]3[C@H]1CC2 QOTITYMKFHXGRE-IYHXRUFHSA-N 0.000 title 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- 238000007796 conventional method Methods 0.000 abstract 2
- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 abstract 2
- HLCRYAZDZCJZFG-BDXSIMOUSA-N (8s,9s,13s,14s)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene Chemical class C1CC2=CC=CC=C2[C@@H]2[C@@H]1[C@@H]1CCC[C@@]1(C)CC2 HLCRYAZDZCJZFG-BDXSIMOUSA-N 0.000 abstract 1
- QZLYKIGBANMMBK-UGCZWRCOSA-N 5α-Androstane Chemical compound C([C@@H]1CC2)CCC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CCC[C@@]2(C)CC1 QZLYKIGBANMMBK-UGCZWRCOSA-N 0.000 abstract 1
- QSHQKIURKJITMZ-OBUPQJQESA-N 5β-cholane Chemical compound C([C@H]1CC2)CCC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CCC)[C@@]2(C)CC1 QSHQKIURKJITMZ-OBUPQJQESA-N 0.000 abstract 1
- JWMFYGXQPXQEEM-NUNROCCHSA-N 5β-pregnane Chemical compound C([C@H]1CC2)CCC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H](CC)[C@@]2(C)CC1 JWMFYGXQPXQEEM-NUNROCCHSA-N 0.000 abstract 1
- 241000193386 Lysinibacillus sphaericus Species 0.000 abstract 1
- 241000203720 Pimelobacter simplex Species 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- -1 alkali metal salt Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 230000022244 formylation Effects 0.000 abstract 1
- 238000006170 formylation reaction Methods 0.000 abstract 1
- CTYOUOHIEXEYAW-MEVSNGMESA-N furostane group Chemical class [C@@H]12C[C@@H]3O[C@H](CCC(C)C)[C@@H](C)[C@@H]3[C@@]1(C)CC[C@H]1[C@H]2CCC2CCCC[C@]12C CTYOUOHIEXEYAW-MEVSNGMESA-N 0.000 abstract 1
- 229910000000 metal hydroxide Inorganic materials 0.000 abstract 1
- 150000004692 metal hydroxides Chemical class 0.000 abstract 1
- 150000003431 steroids Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 150000003509 tertiary alcohols Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
-
- 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
-
- 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)
- Steroid Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL6506542A NL6506542A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1965-05-22 | 1965-05-22 | |
| NL6600548A NL6600548A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1965-05-22 | 1966-01-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1104185A true GB1104185A (en) | 1968-02-21 |
Family
ID=26643890
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB22047/66A Expired GB1104185A (en) | 1965-05-22 | 1966-05-18 | Novel formyl-oestratrienes |
Country Status (5)
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4022769A (en) * | 1974-05-13 | 1977-05-10 | Richardson-Merrell Inc. | Androst-4-en-19-ones |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH454840A (de) * | 1960-10-28 | 1968-04-30 | Ciba Geigy | Verfahren zur Herstellung von Steroid-19-säuren |
-
1965
- 1965-05-22 NL NL6506542A patent/NL6506542A/xx unknown
-
1966
- 1966-01-15 NL NL6600548A patent/NL6600548A/xx unknown
- 1966-05-13 US US549786A patent/US3579543A/en not_active Expired - Lifetime
- 1966-05-18 GB GB22047/66A patent/GB1104185A/en not_active Expired
- 1966-12-28 US US605181A patent/US3431287A/en not_active Expired - Lifetime
-
1967
- 1967-01-06 FR FR90272A patent/FR1507610A/fr not_active Expired
- 1967-01-12 DE DE19671618724 patent/DE1618724A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| FR1507610A (fr) | 1967-12-29 |
| NL6600548A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1967-07-17 |
| NL6506542A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1966-11-23 |
| DE1618724A1 (de) | 1971-04-08 |
| US3431287A (en) | 1969-03-04 |
| US3579543A (en) | 1971-05-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1104185A (en) | Novel formyl-oestratrienes | |
| ES388784A1 (es) | Un procedimiento de preparacion de la 17 alfa - hidroxi - pregna - 4,9 (11)-dieno - 3,20 - diona. | |
| AU229508B2 (en) | 9 fluoro-16 hydroxy steroids ofthe pregnene series their esters, and process for making same | |
| CA485267A (en) | Glucosides from strophanthus sarmentosus and process of making same | |
| AU167346B2 (en) | Anew or improved cyclopentanopolyhydrophenanthrene derivative and methods for its production | |
| AU3598158A (en) | 9 fluoro-16 hydroxy steroids ofthe pregnene series their esters, and process for making same | |
| AU159451B2 (en) | Anew and improved cyclopentanopolyhydrophenanthrene derivative and methods for its production | |
| AU1773353A (en) | Anew or improved cyclopentanopolyhydrophenanthrene derivative and methods for its production | |
| CA539083A (en) | 3.beta., 11.alpha., 21-TRIACYL,17.alpha. HYDROXY PREGNANE,20-ONE | |
| AU219413B2 (en) | Anew and improved flush panel door, and method of making thesame | |
| AU849952A (en) | Evaporator door assembly | |
| AU1471952A (en) | Anew and improved cyclopentanopolyhydrophenanthrene derivative and methods for its production | |
| CA491807A (en) | Window shade pull | |
| CA483327A (en) | Door control mechanisms | |
| CA481772A (en) | Automatic window opener | |
| CA498330A (en) | Aircraft windows and fittings therefor | |
| CA484921A (en) | Door operating mechanism | |
| AU153784B2 (en) | Improvements Relating to Differential Sliding Door Mounting Fittings | |
| CA465855A (en) | Glass feeder shear mechanism actuating means and method | |
| AU215467B2 (en) | The antibiotic paromomycin and process for producing it | |
| CA543646A (en) | Extracting pregnane steroids from fermentation broth | |
| CA487829A (en) | Process for the separation of the hormone and hormone-like components of the pituitary gland | |
| CA482307A (en) | Electromagnetic relay | |
| CA488417A (en) | Compounds of the cyclopentanopolyhydrophenanthrene series and process of making same | |
| ES276601A1 (es) | Procedimiento para la preparación de éteres cicloalcenílicos de 17-betahidroxi-androstanos |