Literature DB >> 20560577

Nickel-catalyzed C-H alkenylation and alkylation of 1,3,4-oxadiazoles with alkynes and styrenes.

Tomoya Mukai1, Koji Hirano, Tetsuya Satoh, Masahiro Miura.   

Abstract

The addition reaction of 1,3,4-oxadiazoles to alkynes via C-H bond cleavage efficiently proceeds in the presence of a nickel catalyst. This direct coupling allows a facile access to alkenyl-substituted oxadiazoles. The reaction with styrenes in place of alkynes is also available to selectively afford the corresponding branched adducts.

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Year:  2009        PMID: 20560577     DOI: 10.1021/jo901350j

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Cobalt(III)-catalyzed synthesis of indazoles and furans by C-H bond functionalization/addition/cyclization cascades.

Authors:  Joshua R Hummel; Jonathan A Ellman
Journal:  J Am Chem Soc       Date:  2014-12-24       Impact factor: 15.419

2.  Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed ortho-Alkylation of Acetanilides.

Authors:  Giacomo E M Crisenza; Olga O Sokolova; John F Bower
Journal:  Angew Chem Int Ed Engl       Date:  2015-10-22       Impact factor: 15.336

3.  Rh(ii)-catalyzed branch-selective C-H alkylation of aryl sulfonamides with vinylsilanes.

Authors:  Supriya Rej; Naoto Chatani
Journal:  Chem Sci       Date:  2019-11-11       Impact factor: 9.825

  3 in total

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