Synthetic Studies toward Potent Cytotoxic Agent Amphidinolide B: Synthesis of the Entire Cl-C13 Moiety of the Bottom Half
- 1 June 1997
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 26 (6) , 565-566
- https://doi.org/10.1246/cl.1997.565
Abstract
Sharpless asymmetric dihydroxylation and Nozaki-Hiyama-Kishi’s Cr(II)-mediated coupling between an α-alkoxyaldehyde and a vinyl iodide are the key steps in the stereoselective synthesis of the entire C1-C13 segment of the bottom-half of amphidinolide B.Keywords
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