TRANSMETALATION OF ALKYLBORANES TO PALLADIUM IN THE SUZUKI COUPLING REACTION PROCEEDS WITH RETENTION OF STEREOCHEMISTRY

Authors
RIDGWAY BH WOERPEL KA
Citation
Bh. Ridgway et Ka. Woerpel, TRANSMETALATION OF ALKYLBORANES TO PALLADIUM IN THE SUZUKI COUPLING REACTION PROCEEDS WITH RETENTION OF STEREOCHEMISTRY, Journal of organic chemistry, 63(3), 1998, pp. 458-460
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of organic chemistry → ACNP
ISSN journal
00223263
Volume
63
Issue
3
Year of publication
1998
Pages
458 - 460
Database
ISI
SICI code
0022-3263(1998)63:3<458:TOATPI>2.0.ZU;2-6
Abstract
Deuterium-labeling experiments demonstrate that the transmetalation st ep of the Suzuki coupling reaction of alkylboranes and alpha-iodoenone s proceeds with retention of stereochemistry.