Zinc chloride catalyzed silylation of alcohols and phenols by hexamethyldisilazane. A highly chemoselective reaction

Article abstract of DOI:10.1080/00397919308011260

Hexamethyldisilazane (HMDS) in presence of a catalytic amount of anhydrous zinc chloride silylates efficiently and selectively different types of alcohols and phenols in refluxing acetonitrile or benzene-acetonitrile. This reagent in presence of anhydrous

Full text of DOI:10.1080/00397919308011260

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Synthetic Communications: An
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Organic Chemistry
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Zinc Chloride Catalyzed
Silylation of Alcohols
and Phenols by
Hexamethyldisilazane. A Highly
Chemoselective Reaction
H. Firouzabadi a & B. Karimi a
a Chemistry Department, College of Sciences, Shiraz
University, Shiraz, Iram
Version of record first published: 23 Sep 2006.
To cite this article: H. Firouzabadi & B. Karimi (1993): Zinc Chloride Catalyzed
Silylation of Alcohols and Phenols by Hexamethyldisilazane. A Highly Chemoselective
Reaction, Synthetic Communications: An International Journal for Rapid
Communication of Synthetic Organic Chemistry, 23:12, 1633-1641
To link to this article: http://dx.doi.org/10.1080/00397919308011260
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