| Literature DB >> 31599297 |
Aurélien Adenot1, Joëlle Char1, Niklas von Wolff1, Guillaume Lefèvre1, Lucile Anthore-Dalion1, Thibault Cantat1.
Abstract
A Pd-catalyzed Hiyama cross-coupling reaction using SO2 is described. The use of silicon-based nucleophiles leads to the formation of allyl sulfones under mild conditions with a broad functional group tolerance. Control experiments coupled with DFT calculations shed light on the key steps of the reaction mechanism, revealing the crucial role of a transient sulfinate anion.Entities:
Year: 2019 PMID: 31599297 DOI: 10.1039/c9cc06858a
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222