T. Shih, Jui-Huang Tseng
Feb 16, 2004
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Journal
Tetrahedron Letters
Abstract
Abstract We reported herein an efficient synthesis of l -allono-1,4-lactone from 2,3:5,6-di- O -isopropylidene- d -mannono-1,4-lactone in five steps. The key feature of this method involved a one-pot, ‘double inversion’ procedure at the stereocenters of C-4 and C-5 of d -mannono-1,4-lactone to afford the target molecule.