The first asymmetric ring-expansion carbonylation of meso-epoxides
- PMID: 22951811
- DOI: 10.1039/c2cc35596e
The first asymmetric ring-expansion carbonylation of meso-epoxides
Abstract
The first asymmetric ring-expansion carbonylation of meso-epoxides to β-lactones is reported. Two structurally diverse chiral Cr(III) chloro complexes in conjunction with Co(2)(CO)(8) were shown to be competent catalytic systems for this transformation, displaying significant levels of asymmetric induction of up to 56% ee.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
