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Synthesis and biological evaluation of himanimide C and unnatural analogues
1Research Chemistry, SYNGENTA Crop Protection AG, CH-4002 Basel, Switzerland. patrice.selles@syngenta.com
Organic Letters
|February 12, 2005
Abstract:
Recently isolated himanimide C (1) can be prepared via a short, flexible, and stereoselective synthesis using a copper-mediated tandem vicinal difunctionalization of dimethyl acetylenedicarboxylate (DMAD, 8) as a key step. The flexibility of the synthesis is exemplified by the preparation of new unnatural himanimide analogues in order to investigate the fungicidal potency of this new family. [structure: see text]
