FACILE INTRAMOLECULAR CYCLOADDITIONS OF 2-(N-ACYLAMINO)-1-THIA-1,3-DIENES

被引：9
|
作者：
BARNISH, IT
FISHWICK, CWG
HILL, DR
机构：
[1] UNIV LEEDS,SCH CHEM,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND
[2] PFIZER LTD,SANDWICH CT13 9NJ,KENT,ENGLAND
来源：
TETRAHEDRON LETTERS | 1991年 / 32卷 / 03期
关键词：
D O I：
10.1016/S0040-4039(00)92640-6
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
2-(N-Acylamino)-1-thia-1,3-dienes, generated via acylation of readily available alpha,beta-unsaturated thioamides, undergo regio- and stereospecific intramolecular Diels-Alder cycloaddition with unactivated olefinic and acetylenic dienophiles to yield polycyclic dihydrothiopyrans.
引用
收藏
页码：405 / 408
页数：4
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