Issue 17, 1998
From the journal:

Chemical Communications

New and efficient selenium reagents for stereoselective selenenylation reactions

Gianfranco Fragale,   Thomas Wirth,   Gianfranco Fragale  and  Markus Neuburger  

Abstract

The simple substitution of an aryl proton by a methoxy substituent improves the selectivity of the stereoselective selenenylation reaction dramatically, leading to addition products with diastereomeric ratios up to 50:1 in the methoxyselenenylation reaction of styrene.

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Article information

DOI
https://doi.org/10.1039/A804264K
Article type
Paper

Chem. Commun., 1998, 1867-1868

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New and efficient selenium reagents for stereoselective selenenylation reactions

G. Fragale, T. Wirth, G. Fragale and M. Neuburger, Chem. Commun., 1998, 1867 DOI: 10.1039/A804264K

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