Literature DB >> 24668255

An efficient ruthenium-catalyzed dehydrogenative synthesis of 2,4,6-triaryl-1,3,5-triazines from aryl methanols and amidines.

Feng Xie1, Mengmeng Chen, Xiaoting Wang, Huanfeng Jiang, Min Zhang.   

Abstract

By using [RuCl2(p-Cymene)]2/Cs2CO3 as an efficient catalyst system, the readily available, inexpensive aryl methanols were firstly employed for dehydrogenative synthesis of aryl substituted 1,3,5-triazine derivatives. Due to the inherent stability of alcohols in contrast with aldehydes, our synthetic protocol is adaptable to a broad substrate scope, there is no need for stringent protection during the whole operation process, and it has the potential to prepare valuable products that are currently inaccessible or challenging to prepare using conventional methods. It is a significantly important complement to the conventional synthetic methodologies.

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Year:  2014        PMID: 24668255     DOI: 10.1039/c3ob42589d

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


  2 in total

1.  TBHP-mediated oxidative synthesis of substituted pyrimido[4,5-d]pyrimidines from N-uracil amidines and methylarenes under metal free conditions.

Authors:  Pradip Debnath
Journal:  RSC Adv       Date:  2019-09-20       Impact factor: 4.036

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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