Diastereoselective synthesis of (2S,5R)-5-hydroxypipecolic acid and 6-substituted derivatives.

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Publication year
2004Source
Organic Letters, 6, 26, (2004), pp. 4941-4ISSN
Publication type
Article / Letter to editor

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Organization
Solid State Chemistry
Synthetic Organic Chemistry
Journal title
Organic Letters
Volume
vol. 6
Issue
iss. 26
Page start
p. 4941
Page end
p. 4
Subject
Molecular Materials; Synthetic Organic ChemistryAbstract
[reaction: see text] Herein, we report a diastereoselective synthesis of the natural product (2S,5R)-5-hydroxypipecolic acid and 6-substituted derivatives thereof. The key step in the synthetic sequence is a novel highly diastereoselective epoxidation reaction of an enantiomerically pure cyclic enamide intermediate.
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