SYNTHESIS OF 20-OXO-DELTA16-STEROIDS BY ELIMINATION OF 17-NITROXY GROUP

被引：9

作者：

HOFMEISTER, H ^{[1
]}

LAURENT, H ^{[1
]}

HOYER, GA ^{[1
]}

WIECHERT, R ^{[1
]}

机构：

[1] SCHERING AG, FORSCH LAB, MULLER STR 170 172, D-1000 BERLIN 65, WEST GERMANY

来源：

CHEMISCHE BERICHTE-RECUEIL | 1974年 / 107卷 / 04期

关键词：

D O I：

10.1002/cber.19741070420

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1235 / 1244

页数：10

共 16 条

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[4] WEAK ACID-CATALYZED REARRANGEMENT OF DIHYDROXYACETONE SIDE CHAIN IN STEROIDS
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[5] EIN NEUER WEG ZUR HERSTELLUNG DER ANDROGEN-HORMONE, AUSGEHEND VOM PREGNANDIOL-(3ALPHA.6ALPHA)-ON-(20)
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[J]. CHEMISCHE BERICHTE-RECUEIL, 1962, 95 (05): : 1094 - &
[6] NEW SYNTHESIS OF 11BETA-HYDROXY-DELTA-16-CORTICOSTEROIDS
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[J]. CHEMISCHE BERICHTE-RECUEIL, 1973, 106 (07): : 2263 - 2267
[7] THE ADRENAL HORMONES AND RELATED COMPOUNDS .2. SYNTHESIS OF 1-DEHYDRO ANALOGS
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (16) : 4438 - 4439
[8] JUNKMANN K, 1960, ARZNEIMITTEL-FORSCH, V10, P921
[9] KOOREMAN HJ, 1971, SYNTHETIC COMMUN, V1, P81
[10] THE ACTION OF ZINC ON THE 20,21-KETOL ACETATE GROUP OF A DELTA-16-PREGNENE
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (10) : 4765 - 4766

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