Synthesis of N-substituted 1,4-dihydroquinolines from the Baylis-Hillman acetates via the successive S(N)2 '-SNAr isomerization strategy

Authors
Kim, JN Kim, HS Gong, JH Chung, YM
Citation
Jn. Kim et al., Synthesis of N-substituted 1,4-dihydroquinolines from the Baylis-Hillman acetates via the successive S(N)2 '-SNAr isomerization strategy, TETRAHEDR L, 42(47), 2001, pp. 8341-8344
Citations number
54
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
47
Year of publication
2001
Pages
8341 - 8344
Database
ISI
SICI code
0040-4039(20011119)42:47<8341:SON1FT>2.0.ZU;2-I
Abstract
1,4-Dihydroquinolines 4a-e were prepared from the reaction of the Baylis-Hi llman acetates of ortho-halobenzaldehydes and benzylamine or cyclohexylamin e via the successive S(N)2'-SNAr isomerization strategy. (C) 2001 Elsevier Science Ltd. All rights reserved.