Preparation of enantiomerically pure 1,3-butanediol from threonine

Article abstract of DOI:10.1080/00397919108021588

Enantiomerically pure R or S 1,3-butanediols were prepared in four steps from L to D threonine by nitrous deamination in the presence of bromide ion followed by esterification and reduction.

Full text of DOI:10.1080/00397919108021588

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Synthetic Communications:
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Preparation of
Enantiomerically Pure 1,3-
Butanediol from Threonine
a
a
Marc Larchevêque , Lengo Mambu & Yves
a
Petit
a
UPR 402 du CNRS , Laboratoire de Chimie ,
Ecole Normale Supérieure, 24, rue Lhomond,
75231, Paris, Cedex, 05, France
Published online: 23 Sep 2006.
To cite this article: Marc Larchevêque , Lengo Mambu & Yves Petit (1991)
Preparation of Enantiomerically Pure 1,3-Butanediol from Threonine, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 21:22, 2295-2300, DOI: 10.1080/00397919108021588
To link to this article: http://dx.doi.org/10.1080/00397919108021588
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