NAOH-PROMOTED CROSS-COUPLING REACTIONS OF ORGANOSILICON COMPOUNDS WITH ORGANIC HALIDES - PRACTICAL ROUTES TO BIARYLS, ALKENYLARENES AND CONJUGATED DIENES

Authors
HAGIWARA E GOUDA K HATANAKA Y HIYAMA T
Citation
E. Hagiwara et al., NAOH-PROMOTED CROSS-COUPLING REACTIONS OF ORGANOSILICON COMPOUNDS WITH ORGANIC HALIDES - PRACTICAL ROUTES TO BIARYLS, ALKENYLARENES AND CONJUGATED DIENES, Tetrahedron letters, 38(3), 1997, pp. 439-442
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
38
Issue
3
Year of publication
1997
Pages
439 - 442
Database
ISI
SICI code
0040-4039(1997)38:3<439:NCROOC>2.0.ZU;2-9
Abstract
The use of NaOH has been found to be extremely effective in promoting the palladium-catalyzed cross-coupling reactions of aryl and alkenylch lorosilanes with organic halides such as aryl bromides and chlorides u nder very mild conditions. Copyright (C) 1996 Elsevier Science Ltd