PALLADIUM-CATALYZED SUZUKI-TYPE SELF-COUPLING OF ARYLBORONIC ACIDS - A MECHANISTIC STUDY

Authors
MORENOMANAS M PEREZ M PLEIXATS R
Citation
M. Morenomanas et al., PALLADIUM-CATALYZED SUZUKI-TYPE SELF-COUPLING OF ARYLBORONIC ACIDS - A MECHANISTIC STUDY, Journal of organic chemistry, 61(7), 1996, pp. 2346-2351
Citations number
34
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of organic chemistry → ACNP
ISSN journal
00223263
Volume
61
Issue
7
Year of publication
1996
Pages
2346 - 2351
Database
ISI
SICI code
0022-3263(1996)61:7<2346:PSSOAA>2.0.ZU;2-D
Abstract
Symmetrical biaryls are formed from arylboronic acids both under tetra kis(triphenylphosphine)palladium and under palladium(II) acetate catal ysis. The principal mechanistic features of these self-couplings have been determined.