Literature DB >> 25349957

Radical reactions of borohydrides.

Takuji Kawamoto1, Ilhyong Ryu.   

Abstract

Borohydrides are an important class of reagents in both organic and inorganic chemistry. Though popular as hydride-transfer reagents for reduction, since earlier work from the 1970s, borohydride reagents have also been known to serve as hydrogen-transfer reagents. In pursuit of greener tin hydride substitutes, recent progress has been made to mediate radical C-C bond forming reactions, including Giese reactions, radical carbonylation and addition to HCHO reactions, with borohydride reagents. This review article focuses on state-of-the-art borohydride based radical reactions, also covering earlier work, kinetics and some DFT calculations with respect to the hydrogen transfer mechanism.

Entities:  

Year:  2014        PMID: 25349957     DOI: 10.1039/c4ob01784f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

1.  A Giese reaction for electron-rich alkenes.

Authors:  Qi Huang; Sankar Rao Suravarapu; Philippe Renaud
Journal:  Chem Sci       Date:  2020-12-17       Impact factor: 9.825

2.  Visible light-mediated difluoroalkylation of electron-deficient alkenes.

Authors:  Vyacheslav I Supranovich; Vitalij V Levin; Marina I Struchkova; Jinbo Hu; Alexander D Dilman
Journal:  Beilstein J Org Chem       Date:  2018-07-02       Impact factor: 2.883

3.  Generation of Alkyl Radicals: From the Tyranny of Tin to the Photon Democracy.

Authors:  Stefano Crespi; Maurizio Fagnoni
Journal:  Chem Rev       Date:  2020-08-06       Impact factor: 60.622

4.  Stereoselective hydrogen atom transfer to acyclic radicals: a switch enabling diastereodivergent borylative radical cascades.

Authors:  Tian Ye; Feng-Lian Zhang; Hui-Min Xia; Xi Zhou; Zhi-Xiang Yu; Yi-Feng Wang
Journal:  Nat Commun       Date:  2022-01-20       Impact factor: 17.694

  4 in total

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