DIELS-ALDER REACTIONS ENHANCED DIASTEREOFACIAL SELECTIVITY IN 5.0 M LICLO4-ET2O APPROACH TO THE CONSTRUCTION OF THE ISOINDOLONE NUCLEUS OF CYTOCHALASANS

被引：21

作者：

GRIECO, PA

BECK, JP

机构：

[1] Department of Chemistry, Indiana University Bloomington

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 46期

关键词：

D O I：

10.1016/S0040-4039(00)60127-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Dienes of type 2 undergo highly diastereoselective Diels-Alder reactions with maleic anhydride in 5.0 M lithium perchlorate-diethyl ether giving rise to isobenzofurandiones which upon exposure to trifluoroacetic acid generate tetrahydroisoindolones.

引用

页码：7367 / 7370

页数：4

共 5 条

[1]

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[5] CYTOCHALASAN SYNTHESIS - MACROCYCLE FORMATION VIA INTRAMOLECULAR DIELS-ALDER REACTIONS [J].

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ACCOUNTS OF CHEMICAL RESEARCH, 1991, 24 (08) :229-235

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