A three-step-one-pot chemo-enzymatic synthesis of epoxyalkanolacylates

Article abstract of DOI:10.1080/00397919808005718

Using the ability of Novozym 435 to catalyze both the perhydrolysis and the interesterification of esters, unsaturated primary alcohols are converted with an ester and hydrogen peroxide to give esters of epoxidized alcohols directly in a convenient three-step-one-pot synthesis with yields of 66-89%.

Full text of DOI:10.1080/00397919808005718

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Synthetic Communications:
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A Three-Step-One-Pot
Chemo-enzymatic Synthesis
of Epoxyalkanolacylates
M. Rüsch gen. Klaas a & S. Warwel a
a Institute for Biochemistry and Technology
of Lipids, Federal Centre for Cereal, Potato
and Lipid Research , Piusallee 68, D - 48143 ,
Münster , Germany
Published online: 21 Aug 2006.
To cite this article: M. Rüsch gen. Klaas & S. Warwel (1998) A Three-Step-
One-Pot Chemo-enzymatic Synthesis of Epoxyalkanolacylates, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 28:2, 251-260, DOI: 10.1080/00397919808005718
To link to this article: http://dx.doi.org/10.1080/00397919808005718
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