109928-28-1Relevant articles and documents
Nickel-catalyzed insertions of vinylidenes into Si-H bonds
Biswas, Sourish,Pal, Sudipta,Uyeda, Christopher
, p. 14175 - 14178 (2020)
A nickel-catalyzed reductive cyclization of 1,1-dichloroalkenyl silanes is reported. The products of this reaction are unsaturated five-or six-membered silacycles. Intermolecular variants are also described, providing access to trisubstituted vinyl silanes that are not accessible by alkyne hydrosilylation or sila-Heck-type processes. A variety of silanes can be utilized, including those that serve as nucleophilic partners in Hiyama cross-coupling reactions. Mechanistic studies using deuterium-labelled silanes are described. This journal is