INTRAMOLECULAR DIELS-ALDER REACTION OF BENZYNES - A NOVEL STRATEGY FOR THE CONSTRUCTION OF TETRAHYDROBENZAZEPINE SKELETONS

Citation
H. Kotsuki et al., INTRAMOLECULAR DIELS-ALDER REACTION OF BENZYNES - A NOVEL STRATEGY FOR THE CONSTRUCTION OF TETRAHYDROBENZAZEPINE SKELETONS, Heterocycles, 38(1), 1994, pp. 31-34
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
03855414
Volume
38
Issue
1
Year of publication
1994
Pages
31 - 34
Database
ISI
SICI code
0385-5414(1994)38:1<31:IDROB->2.0.ZU;2-D
Abstract
Intramolecular Diels-Alder reaction of benzynes, generated from ortho- haloaniline derivatives by the action of lithium 2,2,6,6-tetramethylpi peridide, with furans has been developed as a novel route for the cons truction of tetrahydrobenzazepine skeletons.