RADICAL-INDUCED RING-OPENING OF EPOXIDES - A CONVENIENT ALTERNATIVE TO THE WHARTON REARRANGEMENT

被引：128

作者：

BARTON, DHR ^{[1
]}

MOTHERWELL, RSH ^{[1
]}

MOTHERWELL, WB ^{[1
]}

机构：

[1] CNRS, INST CHIM SUBST NAT, F-91190 GIF SUR YVETTE, FRANCE

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1981年 / 08期

关键词：

D O I：

10.1039/p19810002363

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：2363 / 2367

页数：5

共 36 条

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[6] BARTON DHR, 1979, TETRAHEDRON LETT, P2291
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[8] SYNTHESIS + STEREOCHEMISTRY OF ISOMERIC 16-HYDROXY-17(20)-PREGNENES
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[9] MODIFICATION OF SELDOMYCIN FACTOR-5 AT C-3'
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[J]. JOURNAL OF ANTIBIOTICS, 1978, 31 (05) : 441 - 450
[10] STEROIDAL ALPHA-BETA-EPOXY-KETONES .1. REARRANGEMENT OF 4-ALPHA,5-EPOXY-5-ALPHA-CHOLESTAN-3-ONE AND ITS 4B,5B-ISOMER BY MEANS OF THE BORON TRIFLUORIDE-ETHER COMPLEX
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[J]. JOURNAL OF THE CHEMICAL SOCIETY, 1959, (DEC): : 3919 - 3928

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