OXIRANES IN THE RITTER REACTION - SYNTHESIS OF 6,7-(OR 5,8-)DIMETHOXY-3,4-DIHYDROISOQUINOLINES BY A TANDEM ALKYLATION-CYCLIZATION PROCEDURE

Authors
GLUSHKOV VA SHKLYAEV YV
Citation
Va. Glushkov et Yv. Shklyaev, OXIRANES IN THE RITTER REACTION - SYNTHESIS OF 6,7-(OR 5,8-)DIMETHOXY-3,4-DIHYDROISOQUINOLINES BY A TANDEM ALKYLATION-CYCLIZATION PROCEDURE, Mendeleev communications, (1), 1998, pp. 17-18
Citations number
6
Categorie Soggetti
Chemistry
Journal title
Mendeleev communications → ACNP
ISSN journal
09599436
Issue
1
Year of publication
1998
Pages
17 - 18
Database
ISI
SICI code
0959-9436(1998):1<17:OITRR->2.0.ZU;2-C
Abstract
Treatment of 1,2-(or 1,4)-dimethoxybenzene with isobutylene oxide and an appropriate nitrile RCN in concentrated sulfuric acid leads to 1-R- 6,7-(or -)dimethoxy-3,3-dimethyl-3,4-dihydroisoquinolines.