| Literature DB >> 25123398 |
Yutaro Yamamoto1, Hiroshi Matsubara, Kei Murakami, Hideki Yorimitsu, Atsuhiro Osuka.
Abstract
The palladium-catalyzed silylation of aryl chlorides with silylsilatranes proceeds under activator-free conditions; hence, wide functional group compatibility is displayed and boryl and siloxy groups are able to survive. Experimental and computational studies revealed that smooth transmetalation from the silylsilatrane to the arylpalladium chloride is facilitated by strong interaction between the Lewis acidic silicon and the chloride.Entities:
Keywords: aryl chlorides; palladium; silylation; silylsilatranes; transmetalation
Year: 2014 PMID: 25123398 DOI: 10.1002/asia.201402595
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X