Literature DB >> 26390134

A green and sustainable phosphine-free NHC-ruthenium catalyst for selective oxidation of alcohols to carboxylic acids in water.

Jagadeesh Malineni1, Helmut Keul, Martin Möller.   

Abstract

In this work, we present a new catalytic system for the selective dehydrogenative oxidation of primary alcohols to carboxylic acids using a phosphine-free NHC-ruthenium catalyst in water under mild reaction conditions. With this catalytic system, a variety of primary alcohols have been converted to carboxylic acids respectively, in aqueous media, without using any additional oxidant; the only side product in this reaction is molecular hydrogen. This novel synthetic protocol is applied for direct oxidation of biologically active monosaccharides and polymers with primary alcohol groups in the side chain. The use of water as a solvent and oxygen donor as well as the absence of any toxic oxidizing agent make this atom economical reaction interesting from an environmental point of view.

Entities:  

Year:  2015        PMID: 26390134     DOI: 10.1039/c5dt01358e

Source DB:  PubMed          Journal:  Dalton Trans        ISSN: 1477-9226            Impact factor:   4.390


  3 in total

1.  Iridium-based hydride transfer catalysts: from hydrogen storage to fine chemicals.

Authors:  Zhiyao Lu; Valeriy Cherepakhin; Ivan Demianets; Paul J Lauridsen; Travis J Williams
Journal:  Chem Commun (Camb)       Date:  2018-07-10       Impact factor: 6.222

2.  Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism.

Authors:  Valeriy Cherepakhin; Travis J Williams
Journal:  ACS Catal       Date:  2018-03-26       Impact factor: 13.084

3.  Oxidation of Organic Compounds Using Water as the Oxidant with H2 Liberation Catalyzed by Molecular Metal Complexes.

Authors:  Sayan Kar; David Milstein
Journal:  Acc Chem Res       Date:  2022-07-26       Impact factor: 24.466

  3 in total

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