Palladium-catalyzed carbonylative cross-coupling reactions of pyridine halides and aryl boronic acids: a convenient access to alpha-pyridyl ketones

Authors
Couve-Bonnaire, S Carpentier, JF Mortreux, A Castanet, Y
Citation
S. Couve-bonnaire et al., Palladium-catalyzed carbonylative cross-coupling reactions of pyridine halides and aryl boronic acids: a convenient access to alpha-pyridyl ketones, TETRAHEDR L, 42(22), 2001, pp. 3689-3691
Citations number
15
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
22
Year of publication
2001
Pages
3689 - 3691
Database
ISI
SICI code
0040-4039(20010528)42:22<3689:PCCROP>2.0.ZU;2-U
Abstract
The proper choice of solvent, catalyst precursor and CO pressure enables th e easy and selective transformation of mono- and dihalopyridines into pheny l pyridyl ketones in 81-95%, yields. (C) 2001 Elsevier Science Ltd. All rig hts reserved.