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Centre for Synthesis and Chemical Biology, School of Chemistry and Chemical Biology, University College Dublin, Belfield, Dublin 4, Ireland
E-mail: hasim.ibrahim@ucd.ie
; Fax: +353 1 7161178
; Tel: +353 1 7162978
Chem. Commun., 2012,48, 10138-10140
DOI:
10.1039/C2CC35596E
Received
01 Aug 2012,
Accepted
22 Aug 2012
First published online
22 Aug 2012
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 Co2(CO)8 were shown to be competent catalytic systems for this transformation, displaying significant levels of asymmetric induction of up to 56% ee.