Efficient and Selective Al-Catalyzed Alcohol Oxidation via Oppenauer Chemistry

Christopher R. Graves, Bi-Shun Zeng, and SonBinh T. Nguyen*
Department of Chemistry and Institute for Environmental Catalysis, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113
J. Am. Chem. Soc., 2006, 128 (39), pp 12596–12597
DOI: 10.1021/ja063842s
Publication Date (Web): September 9, 2006
Copyright © 2006 American Chemical Society
*

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, stn@northwestern.edu

Abstract

Abstract Image

A highly active and selective Al-based catalytic Oppenauer (O) oxidation is reported. Quantitative and selective oxidations of a variety of benzylic, propargylic, allylic, and aliphatic primary and secondary alcohols were achieved using nitrobenzaldehyde derivatives as the oxidant and simple aluminum compounds as precatalysts.

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History

  • Published In Issue October 04, 2006
  • Received June 1, 2006

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