THE SYNTHESIS OF HOMOISOTWISTANES BY THE TANDEM WESSELY OXIDATION - DIELS-ALDER REACTION SEQUENCE

被引：11

作者：

BHAMARE, NK ^{[1
]}

GRANGER, T ^{[1
]}

JOHN, CR ^{[1
]}

YATES, P ^{[1
]}

机构：

[1] UNIV TORONTO,LASH MILLER CHEM LABS,TORONTO M5S 1A1,ONTARIO,CANADA

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 35期

关键词：

D O I：

10.1016/0040-4039(91)80006-R

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Wessely oxidation of 5-(2-hydroxyphenyl)-1-pentene and -1-penten-3-ones followed by intramolecular Diels-Alder reactions gave homoisotwistanes; similar treatment of 5-(2-hydroxyphenyl)-3-methylene-1-pentene gave twistane and isotwistane derivatives.

引用

页码：4439 / 4442

页数：4

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