A simple, short, and flexible synthesis of viridiofungin derivatives
Stephen M Goldup1, Christopher J Pilkington, Andrew J P White
1Department of Chemistry, Imperial College London, Exhibition Road, London SW7 2AZ, England.
Abstract:
Described herein is a simple, flexible, and efficient synthesis of the skeleton of the viridiofungins, a family of microbial secondary metabolites. The synthesis utilizes an asymmetric aldol reaction of a chiral oxazolidinone, a diastereoselective alkylation of a chiral 1,3-dioxolan-2-one, and a geometrically selective alkene cross-metathesis reaction as the key C-C bond-forming steps.
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