Improved nickel-catalyzed cross-coupling reaction conditions between ortho-substituted aryl iodides/nonaflates and alkylzinc iodides in solution and in the solid-phase

Authors
Jensen, AE Dohle, W Knochel, P
Citation
Ae. Jensen et al., Improved nickel-catalyzed cross-coupling reaction conditions between ortho-substituted aryl iodides/nonaflates and alkylzinc iodides in solution and in the solid-phase, TETRAHEDRON, 56(25), 2000, pp. 4197-4201
Citations number
13
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
56
Issue
25
Year of publication
2000
Pages
4197 - 4201
Database
ISI
SICI code
0040-4020(20000616)56:25<4197:INCRCB>2.0.ZU;2-P
Abstract
ortho-Substituted aryl iodides and nonaflates undergo nickel-catalyzed cros s-coupling reactions with functionalized alkylzinc iodides in the solid-pha se as well as in solution providing high HPLC purities and good yields. (C) 2000 Elsevier Science Ltd. All rights reserved.