Efficient One-Pot Synthesis of Substituted 4,7-Phenanthroline, Pyrano-[3,2-f]quinoline and Pyrano[3,2-g]quinoline Derivatives by Aza-Diels-Alder Reaction

被引：39

作者：

Majumdar, K. C. ^{[1
]}

Ponra, Sudipta ^{[1
]}

Ghosh, Debankan ^{[1
]}

Taher, Abu ^{[1
]}

机构：

[1] Univ Kalyani, Dept Chem, Kalyani 741235, W Bengal, India

来源：

SYNLETT | 2011年 / 01期

关键词：

multicomponent reaction; BF3 center dot OEt2; 4,7-phenanthroline; pyrano[3,2-f]quinoline; pyrano[3,2-g]quinoline; aromatic aldehyde; phenyl acetylene; FACILE SYNTHESIS; CONJUGATED POLYQUINOLINES; OPTICAL-PROPERTIES; PHASE SYNTHESIS; SOLID-PHASE; IN-VITRO; QUINOLINE; PYRANOQUINOLINE; PYRANO; DOMINO;

D O I：

10.1055/s-0030-1259105

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A mild and efficient method for the synthesis of pyrano[3,2-f] quinoline and 4,7-phenanthroline derivatives via three-component domino reaction of heterocyclic amines, aldehydes, and terminal alkyne using BF3 center dot OEt2 as Lewis acid catalyst is described. The features of this procedure are mild reaction conditions, good to high yields, and operational simplicity.

引用

页码：104 / 110

页数：7

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