Enantioselective hydrolysis of 2,2-disubstituted oxiranes mediated by microsomal epoxide hydrolase

Article abstract of DOI:10.1080/00397919508013848

2-Aryl-2-methyloxiranes are enantioselectively hydrolyzed with microsomal epoxide hydrolase from pig liver to provide 1,2-diols containing a tertiary benzylic alcohol stereogenic centre upto 34% enantiomeric purities.

Full text of DOI:10.1080/00397919508013848

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Synthetic Communications: An
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Enantioselective Hydrolysis
of 2, 2-Disubstituted Oxiranes
Mediated by Microsomal
Epoxide Hydrolase
a
a
Deevi Basavaiah & Sarikonda Bhaskar Raju
a
School of Chemistry, University of Hyderabad,
Hyderabad, 500 046, India
Version of record first published: 23 Sep 2006.
To cite this article: Deevi Basavaiah & Sarikonda Bhaskar Raju (1995):
Enantioselective Hydrolysis of 2, 2-Disubstituted Oxiranes Mediated by Microsomal
Epoxide Hydrolase, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 25:21, 3293-3306
To link to this article: http://dx.doi.org/10.1080/00397919508013848
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