A synthetically useful regioselective epoxide ring-opening procedure

Article abstract of DOI:10.1080/00397919208019093

The reaction of alcohols with epoxides in the presence of boron trifluoride etherate has been investigated and found to proceed with variable regioselectivity depending on the substituents attached to the oxirane ring.

Full text of DOI:10.1080/00397919208019093

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Synthetically Useful
Regioselective Epoxide Ring-
Opening Procedure
Yue-jin Liu a , Ting-yi Chu a & Robert Engel a
a Department of Chemistry and Biochemistry
Queens , College of the City University of New York
Flushing , New York, 11367
Published online: 23 Sep 2006.
To cite this article: Yue-jin Liu , Ting-yi Chu & Robert Engel (1992) A Synthetically
Useful Regioselective Epoxide Ring-Opening Procedure, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 22:16,
2367-2371, DOI: 10.1080/00397919208019093
To link to this article: http://dx.doi.org/10.1080/00397919208019093
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