MICROBIOLOGICAL HYDROXYLATION .18. INTRODUCTION OF 16-ALPHA-HYDROXY-GROUPS,9-ALPHA-HYDROXY GROUPS, AND 3-ALPHA-HYDROXY-GROUPS INTO DIOXYGENATED 5-ALPHA-ANDROSTANES BY FUNGUS DIAPORTHE-CELASTRINA

被引：10

作者：

BELL, AM ^{[1
]}

BOUL, AD ^{[1
]}

JONES, ERH ^{[1
]}

MEAKINS, GD ^{[1
]}

MINERS, JO ^{[1
]}

WILKINS, AL ^{[1
]}

机构：

[1] OXFORD UNIV,DYSON PERRINS LAB,S PARKS RD,OXFORD OX1 3QY,ENGLAND

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1975年 / 14期

关键词：

D O I：

10.1039/p19750001364

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：1364 / 1366

页数：3

共 41 条

[1] STEREOCHEMISTRY OF INTRODUCTION OF 16-ALPHA-METHYL AND 17-ALPHA-HYDROXY GROUPS INTO MOLECULE OF STEROIDS
KRASILNIKOVA, TI
SHNER, VF
TURCHIN, KF
ANISIMOVA, OS
GRINENKO, GS
KHIMIKO-FARMATSEVTICHESKII ZHURNAL, 1982, 16 (05): : 590 - 594
[2] MICROBIOLOGICAL HYDROXYLATION .24. 16-BETA, 18-DIHYDROXYLATION OF OXYGENATED 5-ALPHA-ANDROSTANES BY THE FUNGUS LEPTOPORUS-FISSILIS
DENNY, WA
FREDERICKS, PM
GHILEZAN, I
JONES, ERH
MEAKINS, GD
MINERS, JO
JOURNAL OF CHEMICAL RESEARCH-S, 1980, (01): : 20 - 21
[3] MICROBIOLOGICAL 11BETA-HYDROXYLATION OF 3BETA-HYDROXY-5ALPHA 6ALPHA-EPOXYSTEROIDS
KIESLICH, K
WIEGLEPP, H
CHEMISCHE BERICHTE-RECUEIL, 1971, 104 (01): : 205 - &
[4] MICROBIOLOGICAL HYDROXYLATION OF 5ALPHA,6ALPHA-EPOXY-3BETA-HYDROXY-5ALPHA-PREGNANE-20-ONES WITH FURTHER TRANSFORMATIONS
CLEVE, G
WIEGLEPP, H
KIESLICH, K
HOYER, GA
CHEMISCHE BERICHTE-RECUEIL, 1972, 105 (02): : 658 - &
[5] IMPROVED SULFONATE LEAVING GROUPS FOR DISPLACEMENT AND ELIMINATION OF 3-BETA-HYDROXY AND 11-ALPHA-HYDROXY STEROIDS
ZEHAVI, U
JOURNAL OF ORGANIC CHEMISTRY, 1975, 40 (26): : 3870 - 3873
[6] TRANSFORMED STEROIDS .187. MICROBIOLOGICAL TRANSFORMATION OF 3-BETA-HYDROXY-5-ALPHA-H-PREGNANES TO THEIR DELTA-4-3-KETO-9-ALPHA-HYDROXY DERIVATIVES
VOISHVILLO, NY
TURUTA, AM
KAMERNITSKY, AV
DZHLANTIASHVILI, ND
DACHEVASPASOVA, VK
KHIMIKO-FARMATSEVTICHESKII ZHURNAL, 1992, 26 (02): : 64 - 68
[7] INHIBITION OF STEROL BIOSYNTHESIS BY 9-ALPHA-FLUORO AND 9-ALPHA-HYDROXY DERIVATIVES OF 5-ALPHA-CHOLEST-8(14)-EN-3-BETA-OL-15-ONE
SCHROEPFER, GJ
PARISH, EJ
TSUDA, M
KANDUTSCH, AA
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1979, 91 (02) : 606 - 613
[8] AN EFFICIENT SYNTHESIS OF 3-ALPHA-HYDROXY-5-ALPHA-PREGNA-9(11), 16-DIENE-20-ONE
KIM, WJ
KIM, JH
SHIM, SC
STEROIDS, 1984, 43 (05) : 491 - 497
[9] STUDIES IN THE SYNTHESIS OF CORTISONE .5. ACID REARRANGEMENT OF 9-ALPHA-11-ALPHA-EPOXY-DELTA-7-STEROIDS HAVING HYDROXY-GROUPS OR ACETOXY-GROUPS AT C-(5)
ELKS, J
EVANS, RM
OUGHTON, JF
THOMAS, GH
JOURNAL OF THE CHEMICAL SOCIETY, 1954, (JAN): : 463 - 467
[10] HYDROXY-STEROIDS .18. REACTIONS OF 17 BETA-CHLORO-16 ALPHA, 17 ALPHA-EPOXY-5 ALPHA-ANDROSTANE AND PREPARATION OF 17 BETA-IODO-16 ALPHA, 17 ALPHA-EPOXY-5 ALPHA-ANDROSTANE
DENNY, WA
WICHA, J
PRAGNELL, J
KUMAR, V
MEAKINS, GD
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1972, (04): : 486 - &

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