LEWIS-ACID ASSISTED REACTIONS OF N-(ALPHA-AMINOALKYL)BENZOTRIAZOLES AND UNACTIVATED ALKENES FOR THE FACILE SYNTHESIS OF 4-SUBSTITUTED, 2,4-SUBSTITUTED, AND 3,4-SUBSTITUTED 1,2,3,4-TETRAHYDROQUINOLINES

Authors
KATRITZKY AR NICHOLS DA QI M YANG BZ
Citation
Ar. Katritzky et al., LEWIS-ACID ASSISTED REACTIONS OF N-(ALPHA-AMINOALKYL)BENZOTRIAZOLES AND UNACTIVATED ALKENES FOR THE FACILE SYNTHESIS OF 4-SUBSTITUTED, 2,4-SUBSTITUTED, AND 3,4-SUBSTITUTED 1,2,3,4-TETRAHYDROQUINOLINES, Journal of heterocyclic chemistry, 34(4), 1997, pp. 1259-1262
Citations number
40
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of heterocyclic chemistry → ACNP
ISSN journal
0022152X
Volume
34
Issue
4
Year of publication
1997
Pages
1259 - 1262
Database
ISI
SICI code
0022-152X(1997)34:4<1259:LARONA>2.0.ZU;2-3
Abstract
A range of substituted tetrahydroquinolines have been synthesized from benzotriazole derivatives and unactivated alkenes in the presence of a Lewis acid. These reactions utilize readily available starting mater ials and mild reaction conditions, and give high yields. The reaction mechanisms are discussed.