Literature DB >> 31364360

Reductive Coupling between C-N and C-O Electrophiles.

Rong-De He1, Chun-Ling Li1, Qiu-Quan Pan1, Peng Guo1, Xue-Yuan Liu1, Xing-Zhong Shu1.   

Abstract

The cross-electrophile reaction is a promising strategy for C-C bond formation. Recent studies have focused mainly on reactions with organic halides. Here we report a coupling reaction between C-N and C-O electrophiles that demonstrates the possibility of constructing a C-C bond via C-N and C-O cleavage. Several reactions between benzyl/aryl ammonium salts and vinyl/aryl C-O electrophiles have been studied. Preliminary mechanistic studies revealed that the benzyl ammoniums were activated through a radical mechanism.

Entities:  

Year:  2019        PMID: 31364360     DOI: 10.1021/jacs.9b05224

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Upgrading ketone synthesis direct from carboxylic acids and organohalides.

Authors:  Rehanguli Ruzi; Kai Liu; Chengjian Zhu; Jin Xie
Journal:  Nat Commun       Date:  2020-07-03       Impact factor: 14.919

2.  Ruthenium catalyzed β-selective alkylation of vinylpyridines with aldehydes/ketones via N2H4 mediated deoxygenative couplings.

Authors:  Leiyang Lv; Chao-Jun Li
Journal:  Chem Sci       Date:  2020-12-30       Impact factor: 9.825

  2 in total

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