1-(1-Alkenyl)benzotriazoles: Novel α-hydroxyacyl anion equivalents for the synthesis of α-hydroxy ketones

Article abstract of DOI:10.1080/00397919608004582

α-Lithiated 1-(1-alkenyl)benzotriazoles, generated from the reactions of 1-(1-alkenyl)benzotriazoles with n-BuLi, react with a variety of electrophiles to afford α-substituted 1-(1-alkenyl)benzotriazoles which undergo epoxidation with m-CPBA followed by h

Full text of DOI:10.1080/00397919608004582

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Synthetic Communications: An
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Organic Chemistry
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1-(1-Alkenyl)benzotriazoles:
Novel α-Hydroxyacyl Anion
Equivalents for the Synthesis of
α-Hydroxy Ketones
Alan R. Katritzky a , Kenneth A. Heck a , Jianqing Li a
, Adam Wells a & Catherine Garot a
a Center for Heterocyclic Compounds, Department
of Chemistry , University of Florida , Gainesville, FL,
32611-7200, USA
Published online: 21 Aug 2006.
To cite this article: Alan R. Katritzky , Kenneth A. Heck , Jianqing Li , Adam Wells
& Catherine Garot (1996) 1-(1-Alkenyl)benzotriazoles: Novel α-Hydroxyacyl Anion
Equivalents for the Synthesis of α-Hydroxy Ketones, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:14,
2657-2670, DOI: 10.1080/00397919608004582
To link to this article: http://dx.doi.org/10.1080/00397919608004582
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