A Convenient Nitroxyl Radical Catalyst for the Selective Oxidation of Primary and Secondary Alcohols to Aldehydes and Ketones by O2 and H2O2 under Mild Conditions-Reference-Cited by-同舟云学术

A Convenient Nitroxyl Radical Catalyst for the Selective Oxidation of Primary and Secondary Alcohols to Aldehydes and Ketones by O2 and H2O2 under Mild Conditions

Published:2003-08-26 Issue:6 Volume:7 Page:794-798
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Minisci Francesco¹,Recupero Francesco¹,Rodinò Marianna¹,Sala Massimiliano¹,Schneider Armin¹

Affiliation:

1. Dipartimento di Chimica, Materiali e Ingegneria Chimica “Giulio Natta”, Politecnico di Milano, via Mancinelli 7, 20131 Milano, Italy, Ciba Specialty Chemicals S.p.A., via Pila 6/3 40044 Sasso Marconi (BO) fraz. Pontecchio Marconi, Italy, and Ciba Specialty Chemicals Inc., Building, R.1059.4, 4002 Basel, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op034063o

Reference19 articles.

1. Efficient Mn–Cu and Mn–Co–TEMPO-catalysed oxidation of alcohols into aldehydes and ketones by oxygen under mild conditions

2. A new, highly selective synthesis of aromatic aldehydes by aerobic free-radical oxidation of benzylic alcohols, catalysed by n-hydroxyphthalimide under mild conditions. Polar and enthalpic effects

3. Fast and selective oxidation of primary alcohols to aldehydes or to carboxylic acids and of secondary alcohols to ketones mediated by oxoammonium salts under two-phase conditions

4. A New Modified “Montanari Oxidation Process” by Means of Chlorine Dissolved in the Reaction Solvent as Oxidant and TEMPO as Catalyst: Oxidation of 3-S-Quinuclidinol to 3-Quinuclidinone

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