REACTIVITY OF AMINOETHYLIMIDAZO[1,2-A]PYRIDINE - ACCESS TO AZA-GAMMA-CARBOLINE SERIES

Authors
JOUANISSON A CHAVIGNON O COUQUELET J TEULADE JC CHABARD JL DAUPHIN G
Citation
A. Jouanisson et al., REACTIVITY OF AMINOETHYLIMIDAZO[1,2-A]PYRIDINE - ACCESS TO AZA-GAMMA-CARBOLINE SERIES, Heterocycles, 41(1), 1995, pp. 21-28
Citations number
21
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Heterocycles → ACNP
ISSN journal
03855414
Volume
41
Issue
1
Year of publication
1995
Pages
21 - 28
Database
ISI
SICI code
0385-5414(1995)41:1<21:ROA-AT>2.0.ZU;2-X
Abstract
From 2-(2-aminoethyl)imidazo[1,2-a]pyridine (1), the synthesis of comp ounds possessing the azatetrahydrocarboline moiety was described. The Fujii procedure did not afford the expected tetracyclic compound (5). However, the Pictet-Spengler reaction led to tricyclic aza-gamma-carbo linic type compounds (8a-c).