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Synthesis 2001(12): 1883-1887
DOI: 10.1055/s-2001-17530
DOI: 10.1055/s-2001-17530
PAPER
© Georg Thieme Verlag Stuttgart · New York
A Highly Diastereoselective Synthesis of trans-para-Menthanic Epoxyesters
Further Information
Received
28 March 2001
Publication Date:
12 August 2004 (online)
Publication History
Publication Date:
12 August 2004 (online)
Abstract
A highly diastereoselective two-step synthesis of trans-para-menthanic epoxyesters from parent para-menthenic esters is presented. Among bromolactones or bromohydrines obtained with NBS in the first step, only those, which afforded trans-epoxides, reacted.
Key words
para-menthanic epoxyesters - highly diastereoselective epoxidation - highly diastereoselective synthesis
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