Literature DB >> 25692654

An outstanding catalyst for the oxygen-mediated oxidation of arylcarbinols, arylmethylene and arylacetylene compounds.

G Urgoitia1, R SanMartin, M T Herrero, E Domínguez.   

Abstract

A convenient and sustainable protocol for the aerobic oxidation of benzyl alcohols to carbonyl compounds, based on the use of 1,2,4-triazole-type ligands and nickel(II) bromide, is described. This combination leads to the formation of an exceedingly active, enzyme-like system that allows for other oxidative processes, such as benzylic C-H oxidation and oxygen-mediated cleavage of C-C triple bond, a pioneering procedure for transformation of alkynes into carboxylic acids.

Entities:  

Year:  2015        PMID: 25692654     DOI: 10.1039/c5cc00750j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  A multi pathway coupled domino strategy: I2/TBHP-promoted synthesis of imidazopyridines and thiazoles via sp3, sp2 and sp C-H functionalization.

Authors:  Yishou Wang; Shichen Li; Xinfeng Wang; Yiming Yao; Lei Feng; Chen Ma
Journal:  RSC Adv       Date:  2022-02-17       Impact factor: 3.361

2.  Testing the limits of radical-anionic CH-amination: a 10-million-fold decrease in basicity opens a new path to hydroxyisoindolines via a mixed C-N/C-O-forming cascade.

Authors:  Quintin Elliott; Gabriel Dos Passos Gomes; Christopher J Evoniuk; Igor V Alabugin
Journal:  Chem Sci       Date:  2020-02-21       Impact factor: 9.825

3.  The cumene/O2 system: a very simple tool for the radical chain oxidation of some functional groups.

Authors:  A Malekafzali; K Malinovska; F W Patureau
Journal:  New J Chem       Date:  2017-06-30       Impact factor: 3.591

  3 in total

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