Literature DB >> 22453837

Metal-free TEMPO-catalyzed oxidative C-C bond formation from Csp3-H bonds using molecular oxygen as the oxidant.

Bo Zhang1, Yuxin Cui, Ning Jiao.   

Abstract

An efficient TEMPO-catalyzed oxidative C-C bond formation with two Csp(3)-H bonds using molecular oxygen as the oxidant has been developed. The novel transformation provides a new strategy for the TEMPO-O(2) catalysis to construct C-C bonds. The advantages of this method include: (1) relatively mild and neutral conditions; (2) simplicity and safety of operation; (3) a stoichiometric amount of dangerous oxidants, any transition metals, additives, even solvent, is not required. This journal is © The Royal Society of Chemistry 2012

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Year:  2012        PMID: 22453837     DOI: 10.1039/c2cc30684k

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


  2 in total

1.  A Cu-Catalysed Radical Cross-Dehydrogenative Coupling Approach to Acridanes and Related Heterocycles.

Authors:  Timothy E Hurst; Richard J K Taylor
Journal:  European J Org Chem       Date:  2017-01-06

2.  Selective carboxylation of reactive benzylic C-H bonds by a hypervalent iodine(III)/inorganic bromide oxidation system.

Authors:  Toshifumi Dohi; Shohei Ueda; Kosuke Iwasaki; Yusuke Tsunoda; Koji Morimoto; Yasuyuki Kita
Journal:  Beilstein J Org Chem       Date:  2018-05-16       Impact factor: 2.883

  2 in total

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