2013•The Journal of Organic ChemistryRequires access

Cu-NHC-TEMPO Catalyzed Aerobic Oxidation of Primary Alcohols to Aldehydes

Xiaolong Liu, Qinqin Xia, Yuejiao Zhang, Congyan Chen, Wanzhi Chen

Open publisher page 93 citations

Abstract

Imidazolium salts bearing TEMPO groups react with commercially available copper powder affording Cu-NHC complexes. The in situ generated Cu-NHC-TEMPO complexes are quite efficient catalysts for aerobic oxidation of primary alcohols into aldehydes. The catalyst is easily available, and various primary alcohols were selectively converted to aldehydes in excellent yields.

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What this paper is about

Imidazolium salts bearing TEMPO groups react with commercially available copper powder affording Cu-NHC complexes. The in situ generated Cu-NHC-TEMPO complexes are quite efficient catalysts for aerobic oxidation of primary alcohols into aldehydes. The catalyst is easily available, and various primary alcohols were selectively converted to aldehydes in excellent yields.

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OpenAlex reports 93 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Imidazolium salts bearing TEMPO groups react with commercially available copper powder affording Cu-NHC complexes. The in situ generated Cu-NHC-TEMPO complexes are quite efficient catalysts for aerobic oxidation of primary alcohols into aldehydes. The catalyst is easily available, and various primary alcohols were selectively converted to aldehydes in excellent yields.

Key concepts: Primary (astronomy), Catalysis, Alcohol oxidation, Copper, Chemistry, Organic chemistry, In situ, Aldehyde

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