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The first asymmetric ring-expansion carbonylation of meso-epoxides†
Prasad Ganji,Hasim Ibrahim
Chemical Communications Pub Date : 08/22/2012 00:00:00 , DOI:10.1039/C2CC35596E
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 Co2(CO)8 were shown to be competent catalytic systems for this transformation, displaying significant levels of asymmetric induction of up to 56% ee.

Graphical abstract: The first asymmetric ring-expansion carbonylation of meso-epoxides
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