Literature DB >> 26419899

Silver-catalyzed regioselective [3+2] cycloaddition of arene-diazonium salts with 2,2,2-trifluorodiazoethane (CF3CHN2): a facile access to 2-aryl-5-trifluoromethyltetrazoles.

Zhen Chen1, Shuang-Qing Fan1, Yan Zheng1, Jun-An Ma1.   

Abstract

A silver-catalyzed regioselective [3+2] cycloaddition reaction of arenediazonium salts with 2,2,2-trifluorodiazoethane (CF3CHN2) is reported. Under mild conditions, a series of 2-aryl substituted 5-trifluoromethyltetrazoles were obtained in moderate to excellent yields with wide functional group compatibility. Furthermore, this cycloaddition reaction could also be performed in a one-pot diazotization/cycloaddition sequence from commercially available aniline derivatives.

Entities:  

Year:  2015        PMID: 26419899     DOI: 10.1039/c5cc07324c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Synthesis of 2-aryl-2H-tetrazoles via a regioselective [3+2] cycloaddition reaction.

Authors:  Remi Patouret; Theodore M Kamenecka
Journal:  Tetrahedron Lett       Date:  2016-04-06       Impact factor: 2.415

2.  Activation of Dinitrogen as A Dipolarophile in 1,3-Dipolar Cycloadditions: A Theoretical Study Using Nitrile Imines as "Octet" 1,3-Dipoles.

Authors:  M Merced Montero-Campillo; Ibon Alkorta; José Elguero
Journal:  Sci Rep       Date:  2017-07-21       Impact factor: 4.379

  2 in total

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