RING EXPANSION OF AN ALPHA-BROMOALKYNOL CAMPHOR BY MEANS OF IODINE AND KOSER REAGENT

被引：27

作者：

BOVONSOMBAT, P ^{[1
]}

MCNELIS, E ^{[1
]}

机构：

[1] NYU,DEPT CHEM,NEW YORK,NY 10003

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 27期

关键词：

D O I：

10.1016/S0040-4039(00)79328-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The bromoethynyl adduct of camphor was treated with equimolar amounts of iodine and Koser's reagent (HTIB) to afford in good yield and in good stereospecificity a (Z)-bromoiodoenone, a synthon for enantiospecific syntheses.

引用

页码：4277 / 4280

页数：4

共 9 条

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