Abstract

A powerful approach to cooperative group-transfer catalysis is demonstrated using the Co=Si bond of a cobalt silylene to provide two distinct sites for substrate activation. The orthogonal selectivity of the Co and Si centers enables efficient nitrene-group transfer to carbon monoxide by avoiding poisoning that would result from substrates competing for a single reactive site.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call