Literature DB >> 26477749

NIS-catalyzed oxidative cyclization of alcohols with amidines: a simple and efficient transition-metal free method for the synthesis of 1,3,5-triazines.

Abhishek R Tiwari1, Akash T, Bhalchandra M Bhanage.   

Abstract

An efficient method for the synthesis of 1,3,5-triazines by NIS-catalyzed oxidative cyclization of alcohols with amidines has been developed. The reaction works smoothly under transition-metal free and phosphine-free conditions to afford a wide range of 1,3,5-triazine derivatives in moderate to good yields. The synthetic methodology was achieved via in situ oxidation of alcohols to aldehydes.

Entities:  

Year:  2015        PMID: 26477749     DOI: 10.1039/c5ob01835h

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


  2 in total

1.  Elongated and substituted triazine-based tricarboxylic acid linkers for MOFs.

Authors:  Arne Klinkebiel; Ole Beyer; Barbara Malawko; Ulrich Lüning
Journal:  Beilstein J Org Chem       Date:  2016-10-27       Impact factor: 2.883

2.  Atom-efficient synthesis of 2,4,6-trisubstituted 1,3,5-triazines via Fe-catalyzed cyclization of aldehydes with NH4I as the sole nitrogen source.

Authors:  Jiang Xiao; Shuang Ren; Qiang Liu
Journal:  RSC Adv       Date:  2020-06-09       Impact factor: 3.361

  2 in total

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