Issue 31, 2017

Regioselective hydrosilylation of epoxides catalysed by nickel(ii) hydrido complexes

Abstract

Bench-stable nickel fluoride complexes bearing NNN pincer ligands have been employed as precursors for the regioselective hydrosilylation of epoxides at room temperature. A nickel hydride assisted epoxide opening is followed by the cleavage of the newly formed nickel oxygen bond by σ-bond metathesis with a silane.

Graphical abstract: Regioselective hydrosilylation of epoxides catalysed by nickel(ii) hydrido complexes

Supplementary files

Article information

Article type
Communication
Submitted
03 Mar 2017
Accepted
27 Mar 2017
First published
28 Mar 2017

Chem. Commun., 2017,53, 4308-4311

Regioselective hydrosilylation of epoxides catalysed by nickel(II) hydrido complexes

J. Wenz, H. Wadepohl and L. H. Gade, Chem. Commun., 2017, 53, 4308 DOI: 10.1039/C7CC01655G

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