Literature DB >> 26073645

Silylations of Arenes with Hydrosilanes: From Transition-Metal-Catalyzed C¢X Bond Cleavage to Environmentally Benign Transition-Metal-Free C¢H Bond Activation.

Zheng Xu1, Li-Wen Xu2,3.   

Abstract

The construction of carbon-silicon bonds is highlighted as an exciting achievement in the field of organosilicon chemistry and green chemistry. Recent developments in this area will enable the sustainable chemical conversion of silicon resources into synthetically useful compounds. Especially, the catalytic silylation through C¢H bond activation without directing groups and hydrogen acceptors is one of the most challenging topics in organic chemistry and green chemistry. These remarkable findings on catalytic silylation can pave the way to a more environmentally benign utilization of earth-abundant silicon-based resources in synthetic chemistry.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Keywords:  C-H activation; green chemistry; homogeneous catalysis; silicon; synthetic methods

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Year:  2015        PMID: 26073645     DOI: 10.1002/cssc.201500467

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  1 in total

1.  Rhodium hydride enabled enantioselective intermolecular C-H silylation to access acyclic stereogenic Si-H.

Authors:  Kun An; Wenpeng Ma; Li-Chuan Liu; Tao He; Guiyu Guan; Qing-Wei Zhang; Wei He
Journal:  Nat Commun       Date:  2022-02-14       Impact factor: 17.694

  1 in total

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