N-BENZOYLINDOLE-2,3-QUINODIMETHANE - DIELS-ALDER REACTIVITY AND SYNTHETIC APPLICATIONS FOR [B]ANNELLATED INDOLES

被引：46

作者：

HABER, M ^{[1
]}

PINDUR, U ^{[1
]}

机构：

[1] UNIV MAINZ,DEPT CHEM & PHARM,SAARSTR 21,W-6500 MAINZ 1,GERMANY

来源：

TETRAHEDRON | 1991年 / 47卷 / 10-11期

关键词：

D O I：

10.1016/S0040-4020(01)96104-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Diels-Alder reactivity of in situ generated N-benzoylindole-2,3-quinodimethane has been expanded considerably to include reactions with carbon- and hetero-dienophiles which furnish a variety of [b]annellated indoles as well as functionalized and annellated carbazoles. The frontier molecular orbital theory was found to be a useful model for the prediction of the experimental results under consideration of reactivity aspects.

引用

页码：1925 / 1936

页数：12

共 20 条

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