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Metal- and Base-Free Room-Temperature Amination of Organoboronic Acids with N-Alkyl Hydroxylamines.
Sun, Hong-Bao; Gong, Liang; Tian, Yu-Biao; Wu, Jin-Gui; Zhang, Xia; Liu, Jie; Fu, Zhengyan; Niu, Dawen.
Afiliação
  • Sun HB; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital.
  • Gong L; School of Chemical Engineering, Sichuan University, No. 17 Renmin Nan Road, Chengdu, 610041, China.
  • Tian YB; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital.
  • Wu JG; School of Chemical Engineering, Sichuan University, No. 17 Renmin Nan Road, Chengdu, 610041, China.
  • Zhang X; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital.
  • Liu J; School of Chemical Engineering, Sichuan University, No. 17 Renmin Nan Road, Chengdu, 610041, China.
  • Fu Z; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital.
  • Niu D; School of Chemical Engineering, Sichuan University, No. 17 Renmin Nan Road, Chengdu, 610041, China.
Angew Chem Int Ed Engl ; 57(30): 9456-9460, 2018 07 20.
Article em En | MEDLINE | ID: mdl-29736974
ABSTRACT
We have found that readily available N-alkyl hydroxylamines are effective reagents for the amination of organoboronic acids in the presence of trichloroacetonitrile. This amination reaction proceeds rapidly at room temperature and in the absence of added metal or base, it tolerates a remarkable range of functional groups, and it can be used in the late-stage assembly of two complex units.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article