A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions

Authors
Citation
Af. Littke et Gc. Fu, A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions, J AM CHEM S, 123(29), 2001, pp. 6989-7000
Citations number
119
Categorie Soggetti
Chemistry & Analysis",Chemistry
Journal title
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
ISSN journal
00027863 → ACNP
Volume
123
Issue
29
Year of publication
2001
Pages
6989 - 7000
Database
ISI
SICI code
0002-7863(20010725)123:29<6989:AVCFHR>2.0.ZU;2-5
Abstract
In the presence of Cy2NMe, PdlP(t-Bu)(3) serves as an exceptionally mild an d versatile catalyst for Heck reactions of aryl chlorides and bromides. A s terically and electronically diverse array of aryl bromides, as well as act ivated aryl chlorides, couple with a range of mono- and disubstituted olefi ns at room temperature, furnishing the arylated product with high E/Z stere oselection. The corresponding reactions of a broad spectrum of electron-neu tral and electron-rich aryl chlorides proceed at elevated temperature, also with high selectivity. In terms of scope and mildness, Pd/P(t-Bu)(3)/Cy2NM e represents an advance over previously reported catalysts for these Heck c oupling processes.