Issue 4, 2014

Experimental and computational studies of borohydride catalyzed hydrosilylation of a variety of C[double bond, length as m-dash]O and C[double bond, length as m-dash]N functionalities including esters, amides and heteroarenes

Abstract

Sodium borohydride and a series of related borohydrides catalyze a transition metal-free hydrosilylation of a variety of C[double bond, length as m-dash]O and C[double bond, length as m-dash]N functionalities under mild conditions. Importantly, many of these reactions are possible using the cheap and environmentally benign hydrosilane polymethylhydrosiloxane. A mechanism is proposed based on experimental and computational results.

Graphical abstract: Experimental and computational studies of borohydride catalyzed hydrosilylation of a variety of C [[double bond, length as m-dash]] O and C [[double bond, length as m-dash]] N functionalities including esters, amides and heteroarenes

Supplementary files

Article information

Article type
Paper
Submitted
26 Nov 2013
Accepted
13 Feb 2014
First published
24 Feb 2014

New J. Chem., 2014,38, 1694-1700

Experimental and computational studies of borohydride catalyzed hydrosilylation of a variety of C[double bond, length as m-dash]O and C[double bond, length as m-dash]N functionalities including esters, amides and heteroarenes

M. G. Manas, L. S. Sharninghausen, D. Balcells and R. H. Crabtree, New J. Chem., 2014, 38, 1694 DOI: 10.1039/C3NJ01485A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements