Stereoselective synthesis of cis-fused hexahydro-isoindolones

被引：1

作者：

Rehn, S ^{[1
]}

Ofial, AR ^{[1
]}

Polborn, K ^{[1
]}

Mayr, H ^{[1
]}

机构：

[1] Univ Munich, Dept Chem, Butenandtstr 5-13,Haus F, D-81377 Munich, Germany

来源：

ARKIVOC | 2004年

关键词：

Diels-Alder reactions; isoindolones; lactams; stereoselectivity; x-ray analysis;

D O I：

10.3998/ark.5550190.0005.312

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Allylamines, readily accessible by ene reactions of N,N-dibenzyliminium pentachlorostannates with 1,3-enynes, undergo domino reactions with maleic anhydride or maleic imide to give cis-fused hexahydroisoindolones, which were characterized by x-ray analysis.

引用

页码：120 / 131

页数：12

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