Literature DB >> 28121453

Carbene-Catalyzed Reductive Coupling of Nitrobenzyl Bromide and Nitroalkene via the Single-Electron-Transfer (SET) Process and Formal 1,4-Addition.

Yuhuang Wang1, Yu Du1, Xuan Huang1, Xingxing Wu1, Yuexia Zhang1, Song Yang2, Yonggui Robin Chi1,2.   

Abstract

A carbene-catalyzed reductive 1,4-addition of nitrobenzyl bromides to nitroalkenes is disclosed. The reaction proceeds via a carbene-enabled single-electron-transfer process that generates radicals as key intermediates. The present study expands the potentials of carbene catalysis and offers unusual transformations for common substrates in organic synthesis.

Entities:  

Year:  2017        PMID: 28121453     DOI: 10.1021/acs.orglett.6b03792

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  Single-electron Carbene Catalysis in Redox Processes.

Authors:  Anna V Bay; Karl A Scheidt
Journal:  Trends Chem       Date:  2022-02-11

2.  Three-component carboacylation of alkenes via cooperative nickelaphotoredox catalysis.

Authors:  Dingyi Wang; Lutz Ackermann
Journal:  Chem Sci       Date:  2022-05-30       Impact factor: 9.969

3.  Critical Assessment of the Reducing Ability of Breslow-type Derivatives and Implications for Carbene-Catalyzed Radical Reactions*.

Authors:  Ludivine Delfau; Samantha Nichilo; Florian Molton; Julie Broggi; Eder Tomás-Mendivil; David Martin
Journal:  Angew Chem Int Ed Engl       Date:  2021-11-15       Impact factor: 16.823

4.  SET processes in Lewis acid-base reactions: the tritylation of N-heterocyclic carbenes.

Authors:  Zhaowen Dong; Cristian Pezzato; Andrzej Sienkiewicz; Rosario Scopelliti; Farzaneh Fadaei-Tirani; Kay Severin
Journal:  Chem Sci       Date:  2020-04-09       Impact factor: 9.825

  4 in total

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