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Butane-2,3-diacetal-desymmetrized glycolic acid—a new building block for the stereoselective synthesis of enantiopure α-hydroxy acids

Abstract:
According to a chiral memory protocol, a chiral glycolic acid equivalent, the butane-2,3-diacetal-desymmetrized glycolate 2, is obtained from chiral 3-halopropane-1,2-diols 1. Compound 2 is a new and effective building block for the synthesis of mono- and dialkylated α-hydroxy acids 3, which constitute a biologically and pharmacologically important structural motif.
Publication status:
Published
Peer review status:
Peer reviewed

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Publisher:
Wiley-VCH
Journal:
Angewandte Chemie (International ed. in English) More from this journal
Volume:
40
Issue:
15
Pages:
2906-2909
Publication date:
2001-08-01
DOI:
EISSN:
1521-3773
ISSN:
1433-7851


Language:
English
Keywords:
UUID:
uuid:9999de0d-2090-447e-a814-71ff6dfb49ef
Local pid:
pubs:52090
Source identifiers:
52090
Deposit date:
2012-12-19
ARK identifier:

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