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
收藏
页码：8925 / 8929
页数：5
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