Literature DB >> 27073988

Divergent copper-mediated dimerization and hydroxylation of benzamides involving C-H bond functionalization.

Mingliang Wang1, Yimin Hu2, Zhe Jiang1, Hong C Shen2, Xun Sun3.   

Abstract

Convenient methods were developed for copper-mediated oxidative C-H activation of aminoquinoline benzamides. The reaction conditions can be tuned to give either hydroxylation or dimerization compounds as the major products efficiently. Preliminary mechanistic studies suggested that different coordination states of copper may lead to different reaction outcomes.

Entities:  

Year:  2016        PMID: 27073988     DOI: 10.1039/c6ob00392c

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


  2 in total

1.  A redox-neutral catechol synthesis.

Authors:  Qian Wu; Dingyuan Yan; Ying Chen; Ting Wang; Feng Xiong; Wei Wei; Yi Lu; Wei-Yin Sun; Jie Jack Li; Jing Zhao
Journal:  Nat Commun       Date:  2017-01-27       Impact factor: 14.919

2.  Assessment of aromatic amides in printed food contact materials: analysis of potential cleavage to primary aromatic amines during simulated passage through the gastrointestinal tract.

Authors:  Nataly Bittner; Andy Boon; Evert H Delbanco; Christof Walter; Angela Mally
Journal:  Arch Toxicol       Date:  2022-03-05       Impact factor: 6.168

  2 in total

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