Efficient construction of 1,2-dihydroquinoline and 1,2,3,4-tetrahydroquinoline rings using tandem Michael-aldol reaction

被引：49

作者：

Makino, K

Hara, O

Takiguchi, Y

Katano, T

Asakawa, Y

Hatano, K

Hamada, Y ^{[1
]}

机构：

[1] Chiba Univ, Grad Sch Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan

[2] Meijo Univ, Fac Pharm, Tempaku Ku, Nagoya, Aichi 4608503, Japan

[3] Nagoya City Univ, Grad Sch Pharmaceut Sci, Mizuho Ku, Nagoya, Aichi 4678603, Japan

来源：

TETRAHEDRON LETTERS | 2003年 / 44卷 / 50期

关键词：

1,2-dihydroquinoline; 1,2,3,4-tetrahydroquinoline; tandem Michael-aidol reaction;

D O I：

10.1016/j.tetlet.2003.10.011

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

1,2-Dihydroquinolines and a 1,2,3,4-tetrahydroquinoline were efficiently constructed using tandem Michael-aldol reaction starting from N-protected o-aminobenzaldehydes and alpha,beta-unsaturated carbonyl compounds in good yield. (C) 2003 Elsevier Ltd. All rights reserved.

引用

页码：8925 / 8929

页数：5

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