Issue 13, 2000
From the journal:

Chemical Communications

Methyltrioxorhenium-catalyzed epoxidations in ionic liquids

Gregory S. Owensa  and  Mahdi M. Abu-Omar*a  

* Corresponding authors

a Department of Chemistry and Biochemistry, University of California, Los Angeles, CA, USA.
E-mail: mao@chem.ucla.edu

Abstract

Alkenes and allylic alcohols have been epoxidized in an ambient-temperature ionic liquid for the first time using methyltrioxorhenium (MTO) and urea hydrogen peroxide; excellent conversions and selectivities for the epoxides of a wide number of substrates were observed.

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Article information

DOI
https://doi.org/10.1039/B001661F
Article type
Communication
Submitted
28 Feb 2000
Accepted
11 May 2000
First published
13 Jun 2000

Chem. Commun., 2000, 1165-1166

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Methyltrioxorhenium-catalyzed epoxidations in ionic liquids

G. S. Owens and M. M. Abu-Omar, Chem. Commun., 2000, 1165 DOI: 10.1039/B001661F

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