Format

Send to

Choose Destination
Angew Chem Int Ed Engl. 2009;48(11):1896-8. doi: 10.1002/anie.200805604.

Asymmetric hydroboration of 1,1-disubstituted alkenes.

Author information

1
School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK.

Abstract

A breakthrough in the asymmetric hydroboration of notoriously difficult 1,1-disubstituted alkenes using a new family of highly effective hydroboration reagents is described (see scheme). The intermediate boranes can be oxidized to alcohols or used in Suzuki-Miyaura cross-coupling reactions.

PMID:
19185046
DOI:
10.1002/anie.200805604
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center