Chimie organique: recherches en cours
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Stereoselective Total Synthesis of Proposed Structure of Stagonolide D

Avula Satya Kumar, Jayprakash Narayan Kumar, Boddu Shashi Kanth, Digambar Balaji Shinde and Biswanath Das

The stereoselective total synthesis of the proposed structure of naturally occurring nonenolide stagonolide D has been achieved using D-mannitol as the starting material. The latter has been utilized for the preparation of both the olefinic alcohol segment and the olefinic acid segment of the target molecule. The synthetic sequence involves asymmetric epoxidation and ring-closing metathesis as the key steps.