Issue 11, 2012

Transition metal-free, NaOtBu-O2-mediated one-pot cascade oxidation of allylic alcohols to α,β-unsaturated carboxylic acids

Abstract

We developed a protocol for the transition metal-free, direct oxidation of allylic alcohols using the simple base NaOtBu under an oxygen atmosphere. The NaOtBu–O2 system exhibited unprecedented activity and selectivity in this oxidation reaction. In particular, a competing epoxidation reaction was suppressed under these conditions.

Graphical abstract: Transition metal-free, NaOtBu-O2-mediated one-pot cascade oxidation of allylic alcohols to α,β-unsaturated carboxylic acids

Supplementary files

Article information

Article type
Communication
Submitted
16 May 2012
Accepted
03 Sep 2012
First published
04 Sep 2012

Green Chem., 2012,14, 2996-2998

Transition metal-free, NaOtBu-O2-mediated one-pot cascade oxidation of allylic alcohols to α,β-unsaturated carboxylic acids

S. M. Kim, Y. S. Kim, D. W. Kim and J. W. Yang, Green Chem., 2012, 14, 2996 DOI: 10.1039/C2GC36203A

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