Synthesis of N-substituted 1,4-dihydroquinolines from the Baylis-Hillman acetates via the successive SN2′-SNAr isomerization strategy

被引：90

作者：

Kim, JN ^{[1
]}

Kim, HS

Gong, JH

Chung, YM

机构：

[1] Chonnam Natl Univ, Dept Chem, Kwangju 500757, South Korea

[2] Chonnam Natl Univ, Inst Basic Sci, Kwangju 500757, South Korea

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 47期

关键词：

dihydroquinoline; isomerization; Baylis-Hillman reaction;

D O I：

10.1016/S0040-4039(01)01791-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

1,4-Dihydroquinolines 4a-e were prepared from the reaction of the Baylis-Hillman acetates of ortho-halobenzaldehydes and benzylamine or cyclohexylamine via the successive S(N)2'-SNAr isomerization strategy. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：8341 / 8344

页数：4

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