Literature DB >> 15012081

Microwave-assisted amination from aryl triflates without base and catalyst.

Gang Xu1, Yan-Guang Wang.   

Abstract

[reaction: see text] Aryl triflates are effectively converted to the corresponding anilines under microwave irradiation in 1-methyl-2-pyridone (NMP) without base and catalyst. Aryl triflates substituted with both electron-poor and electron-rich groups give good to excellent yields. It is noteworthy that the halogenated aryl triflates can chemoselectively react with amines to afford halogenated anilines.

Entities:  

Year:  2004        PMID: 15012081     DOI: 10.1021/ol049963j

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


  2 in total

1.  Convenient Method of Synthesizing Aryloxyalkyl Esters from Phenolic Esters Using Halogenated Alcohols.

Authors:  Xueyang Jiang; Junting Zhou; Yue Zhou; Haopeng Sun; Jian Xu; Feng Feng; Wei Qu
Journal:  Molecules       Date:  2018-07-13       Impact factor: 4.411

2.  Microwave-assisted amination of a chloropurine derivative in the synthesis of acyclic nucleoside analogues.

Authors:  Andreas Lanver; Hans-Günther Schmalz
Journal:  Molecules       Date:  2005-02-28       Impact factor: 4.411

  2 in total

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