 |
| LETTER | Synlett 2007: 1383-1386 DOI: 10.1055/s-2007-980344 |
© Georg Thieme Verlag Stuttgart · New York
|
 |
Highly Stereoselective Cobalt-Catalyzed Allylation of Functionalized Diarylzinc Reagents
|
| Guillaume Dunet, Paul Knochel* |
Department Chemie und Biochemie, Ludwig-Maximilians-Universität München, Butenandtstraße 5-13, 81377 München, Germany Fax: +49(89)218077680; e-Mail: Paul.Knochel@cup.uni-muenchen.de;
|
|
Received
27 February 2007 |
Abstract
Functionalized diarylzinc reagents react readily with allylic chlorides or phosphates in the presence of Co(acac)2 (10 mol%) to give the SN2 products in high yields and with retention of the double-bond configuration. Functionalities like ester, ketone, or cyano are tolerated. Key words
catalysis - allylation - cobalt catalysis - organozinc reagents - stereoselective cross-coupling - nocarasin C
|  |