| Literature DB >> 32691600 |
Fang-Fang Feng1, Jun-Kuan Li1, Xuan-Yu Liu1, Fa-Guang Zhang1,2, Chi Wai Cheung1,2, Jun-An Ma1,2.
Abstract
The general synthesis of fully substituted N2-aryl-1,2,3-triazoles is hitherto challenging compared with that of the N1-aryl counterparts. Herein, we describe a Cu-catalyzed annulation reaction of azirines and aryldiazonium salts. This regiospecific method allows access to a broad spectrum of tri-carbo N2-aryl-1,2,3-triazoles substituted with diverse aryl and alkyl moieties. Its utility is highlighted by the synthesis of several triazole precursors applicable in drug discovery, as well as novel chiral binaphthyl ligands bearing triazole moieties.Entities:
Year: 2020 PMID: 32691600 DOI: 10.1021/acs.joc.0c01433
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354