Literature DB >> 25584697

A synthetic approach to N-aryl carbamates via copper-catalyzed Chan-Lam coupling at room temperature.

Soo-Yeon Moon1, U Bin Kim, Dan-Bi Sung, Won-Suk Kim.   

Abstract

A mild and efficient synthesis of N-arylcarbamates was achieved by reacting azidoformates with boronic acids in the presence of 10 mol % of copper chloride catalyst. The reaction proceeds readily in an open flask at room temperature without additional base, ligand, or additive. Rapid access to urea analogues via a two-step one-pot procedure is enabled by reacting N-arylcarbamates with aluminum-amine complexes. In addition, among several boronic acid derivatives prepared, dimethylphenyl boronate was found to react rapidly in its reaction with benzyl azidoformate, invoking in situ generation of this species in the catalytic cycle.

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Year:  2015        PMID: 25584697     DOI: 10.1021/jo502828r

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Chan-Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical N-arylsulfamides.

Authors:  Suk-Young Won; Seo-Eun Kim; Yong-Ju Kwon; Inji Shin; Jungyeob Ham; Won-Suk Kim
Journal:  RSC Adv       Date:  2019-01-18       Impact factor: 4.036

  1 in total

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