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Enantioselective total synthesis of (S)-nakinadine B†‡
Yuvraj Garg,Satyendra Kumar Pandey
RSC Advances Pub Date : 03/03/2016 00:00:00 , DOI:10.1039/C6RA03915D
Abstract

A novel approach for the synthesis of α-phenyl-β2-amino acid core unit 1 and its application to the total synthesis of (S)-nakinadine B 3, a marine natural product, is described. The synthesis utilizes the optimized combination of diphenylprolinol silyl ether mediated asymmetric Michael addition and a proline catalyzed aminoxylation reactions as key steps.

Graphical abstract: Enantioselective total synthesis of (S)-nakinadine B
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