Convenient and Efficient Preparation of N-Protected (α-Aminoacyl)oxy-Substituted Terpenes and Alkanes

Alan R. Katritzky; Parul Angrish

doi:10.1055/s-2006-950349

PAPER

Convenient and Efficient Preparation of N-Protected (α-Aminoacyl)oxy-Substituted Terpenes and Alkanes

Alan R. Katritzky*, Parul Angrish
Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, FL 32611-7200, USA
e-Mail: katritzky@chem.ufl.edu;

Abstract

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Abstract

Chiral N-protected (α-aminoacyl)oxy-substituted terpenes and alkanes, including diastereomeric analogues, are conveniently and efficiently prepared from the corresponding readily available chiral and racemic 1-{[(benzyloxycarbonyl)amino]acyl}benzotriazoles under microwave irradiation with naturally occurring terpene alcohols or alkanols.

Key words

N-protected [(α-aminoacyl)oxy]benzotriazoles - alcohols - O-acylation - chirality - microwave

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References

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