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

[21] PHOTOEXCITED NITROBENZENE FOR BENZYLIC HYDROXYLATION - SYNTHESIS OF 17BETA-ACETOXY-9ALPHA-HYDROXY-3-METHOXY-ESTRA-1,3,5(10)-TRIENE
LIBMAN, J
BERMAN, E
TETRAHEDRON LETTERS, 1977, (25) : 2191 - 2192
[22] STEROIDS .32. INTRODUCTION OF THE 11-KETO AND 11-ALPHA-HYDROXY GROUPS INTO RING C UNSUBSTITUTED STEROIDS .5. DELTA-8-7-KETONES
DJERASSI, C
MANCERA, O
VELASCO, M
STORK, G
ROSENKRANZ, G
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (13) : 3321 - 3323
[23] STEROIDS AS IMMUNOCHEMICAL PROBES .1. INFLUENCE OF OXO-GROUPS, AND-OR HYDROXY-GROUPS AT C-16-C-17 OF ESTROGENS ON AFFINITY TO ANTI-ESTRONE-17ALPHA-ANTISERA, ANTI-ESTRADIOL-17ALPHA-ANTISERA AND ANTI-ESTRADIOL-17BETA-ANTISERA
KUSS, E
GOEBEL, R
ENDERLE, H
HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1973, 354 (04): : 347 - 364
[24] STEROIDS .45. INTRODUCTION OF THE 11-KETO AND 11-ALPHA-HYDROXY GROUPS INTO RING-C UNSUBSTITUTED STEROIDS .8. PERFORMIC ACID OXIDATION OF 7,9(11)-DIENES
DJERASSI, C
MANCERA, O
ROMO, J
ROSENKRANZ, G
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (14) : 3505 - 3510
[25] STEROIDS .31. INTRODUCTION OF THE 11-KETO AND 11-ALPHA-HYDROXY GROUPS INTO RING-C UNSUBSTITUTED STEROIDS .4. SATURATED 7,11-DIONES
ROMO, J
STORK, G
ROSENKRANZ, G
DJERASSI, C
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (11) : 2918 - 2920
[26] Aziridination of alpha,beta-unsaturated esters bearing allylic hydroxy groups with 3-acetoxyaminoquinazolinones: Evidence for a mechanism comprising Michael addition-S(N)2 nucleophilic displacement of acetoxy for aziridination of alpha,beta-unsaturated esters
Atkinson, RS
Williams, PJ
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1996, (16): : 1951 - 1959
[27] APPLICATION OF THE EXCITON CHIRALITY METHOD FOR THE STEREOCHEMICAL ASSIGNMENT OF REMOTE GROUPS - DETERMINATION OF THE ALPHA-CONFIGURATION OR BETA-CONFIGURATION OF A 2-HYDROXY-SUBSTITUENT IN 2,17 AND 2,16-DIHYDROXY-A-NOR-5ALPHA-ANDROSTANE AND ANDROESTRANE DERIVATIVES
CANCEILL, J
COLLET, A
JACQUES, J
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1982, (01): : 83 - 89
[28] INTRODUCTION OF THE 11-KETO AND 11-ALPHA-HYDROXY GROUPS INTO RING-C UNSUBSTITUTED STEROIDS .7. STEROIDS .42. STEROIDAL SAPOGENINS .26. THE CHEMICAL REDUCTION OF DELTA-8-11-KETO AND OF SATURATED 11-KETO STEROIDS - A NEW APPROACH TO 11-KETO AND 11-ALPHA-HYDROXY STEROIDS
SONDHEIMER, F
MANCERA, O
ROSENKRANZ, G
DJERASSI, C
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (06) : 1282 - 1285
[29] STEROIDAL ANALOGS OF UNNATURAL CONFIGURATION .18. CONFORMATIONAL-ANALYSIS OF 17-BETA-HYDROXY-4,4,9-TRIMETHYL-9-BETA, 10-ALPHA-ESTR-5-EN-3-ONE AND THE DERIVED 2-ALPHA-BROMO-COMPOUNDS AND 2-BETA-BROMO-COMPOUNDS
BULL, JR
PACHTER, R
TUINMAN, A
VANROOYEN, PH
TETRAHEDRON, 1984, 40 (04) : 777 - 784
[30] STEROIDAL SAPOGENINS .23. INTRODUCTION OF THE 11-KETO AND 11-ALPHA-HYDROXY GROUPS INTO RING-C UNSUBSTITUTED STEROIDS .6. NEW APPROACH TO 11-OXYGENATED STEROIDS
SONDHEIMER, E
YASHIN, R
ROSENKRANZ, G
DJERASSI, C
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (10) : 2696 - 2697

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