Literature DB >> 28436219

Room-Temperature CuI-Catalyzed Amination of Aryl Iodides and Aryl Bromides.

Xiaomei Ding1, Manna Huang1, Zhou Yi1, Dongchen Du1, Xinhai Zhu1, Yiqian Wan1.   

Abstract

A general and effective CuI/N',N'-diaryl-1H-pyrrole-2-carbohydrazide catalyst system was developed for the amination of aryl iodides and bromides at room temperature with good chemoselectivity between -OH and -NH2 groups. Only 5 mol % of CuI and ligands was needed in this protocol to effect the amination of various aryl bromides and aryl iodides with a wide range of aliphatic and aryl amines (1.3 equiv).

Entities:  

Year:  2017        PMID: 28436219     DOI: 10.1021/acs.joc.7b00290

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


  3 in total

1.  Electrochemically Enabled, Nickel-Catalyzed Amination.

Authors:  Chao Li; Yu Kawamata; Hugh Nakamura; Julien C Vantourout; Zhiqing Liu; Qinglong Hou; Denghui Bao; Jeremy T Starr; Jinshan Chen; Ming Yan; Phil S Baran
Journal:  Angew Chem Int Ed Engl       Date:  2017-09-14       Impact factor: 15.336

2.  Triarylmethane Fluorophores Resistant to Oxidative Photobluing.

Authors:  Alexey N Butkevich; Mariano L Bossi; Gražvydas Lukinavičius; Stefan W Hell
Journal:  J Am Chem Soc       Date:  2019-01-02       Impact factor: 15.419

3.  N-Cyanorhodamines: cell-permeant, photostable and bathochromically shifted analogues of fluoresceins.

Authors:  Lukas Heynck; Jessica Matthias; Mariano L Bossi; Alexey N Butkevich; Stefan W Hell
Journal:  Chem Sci       Date:  2022-06-27       Impact factor: 9.969

  3 in total

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