Lipase-mediated resolutions of 1-aryl-3-buten-1-ols

Article abstract of DOI:10.1080/00397919708003359

Racemic mixtures of 1-aryl-3-buten-1-ols were separated with high enantioselectivity by a lipase-mediated acetylation with vinyl acetate. The effects of the nature, position, and spatial requirements of the phenyl-ring substituents on the separation efficacy were investigated.

Full text of DOI:10.1080/00397919708003359

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Lipase-Mediated Resolutions of
1
-Aryl-3-Buten-1-ols
a
b
Zbigniew Chalecki , Eryka Guibé-Jampe & Jan
a
Plenkiewicz
a
Faculty of Chemistry , Warsaw University of
Technology , 00-664, Warsaw, Poland
b
Institut de Chimie Moleculaire d'Orsay, Universite
Paris-Sud , France
Published online: 22 Aug 2006.
To cite this article: Zbigniew Chalecki , Eryka Guibé-Jampe & Jan Plenkiewicz (1997)
Lipase-Mediated Resolutions of 1-Aryl-3-Buten-1-ols, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 27:7,
1217-1222, DOI: 10.1080/00397919708003359
To link to this article: http://dx.doi.org/10.1080/00397919708003359
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