PREPARATION AND REACTIONS OF BENZOFURANO-3-SULFOLENES, INDOLO-3-SULFOLENES, AND BENZOTHIENO-3-SULFOLENES

Authors
Citation
Cw. Ko et Ts. Chou, PREPARATION AND REACTIONS OF BENZOFURANO-3-SULFOLENES, INDOLO-3-SULFOLENES, AND BENZOTHIENO-3-SULFOLENES, Journal of organic chemistry, 63(14), 1998, pp. 4645-4653
Citations number
53
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00223263
Volume
63
Issue
14
Year of publication
1998
Pages
4645 - 4653
Database
ISI
SICI code
0022-3263(1998)63:14<4645:PAROBI>2.0.ZU;2-7
Abstract
Benzofurano-, N-tosylindolo-, and benzothieno-3-sulfolenes have been p repared efficiently via their dihydro analogues. These fused 3-sulfole nes serve as ideal precursors for the corresponding heteroaromatic o-q uinodimethanes. Derivatives of these 3-sulfolenes bearing bromo or alk yl group substitution from which substituted heteroaromatic o-quinodim ethanes are generated have also been synthesized.