The Baylis-Hillman Bromides as Versatile Synthons: A Facile One-Pot Synthesis of Indolizine and Benzofused Indolizine Frameworks

被引：77

作者：

Basavaiah, Deevi ^{[1
]}

Devendar, Badugu ^{[1
]}

Lenin, Dandamudi V. ^{[1
]}

Satyanarayana, Tummanapalli ^{[1
]}

机构：

[1] Univ Hyderabad, Sch Chem, Hyderabad 500046, Andhra Pradesh, India

来源：

SYNLETT | 2009年 / 03期

关键词：

Baylis-Hillman bromides; 1,5-cyclization strategy; indolizines; benzofused indolizines; quinoline; isoquinoline; CARBINOLAMINE TUMOR INHIBITORS; C-C BONDS; SUBSTITUTED INDOLIZINES; TANDEM CONSTRUCTION; EFFICIENT SYNTHESIS; ACTIVATED ALKENES; ADDUCTS; ACETATES; DERIVATIVES; REGIOSELECTIVITY;

D O I：

10.1055/s-0028-1087533

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A facile one-pot synthesis of indolizine, benzofused indolizines [pyrrolo[1,2-a]quinoline and pyrrolo[1,2-a]isoquinoline] derivatives from the Baylis Hillman (B II) bromides, via an interesting strategy involving 1,5-cyclization of nitrogen ylides has been described.

引用

页码：411 / 416

页数：6

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