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Enantioselective Nickel-Catalyzed Denitrogenative Transannulation En Route to N-N Atropisomers.
Ge, Fang-Bei; Lu, Chuan-Jun; Chen, Xiao; Yao, Wang; An, Mei; Jiang, Yu-Kun; Xu, Li-Ping; Liu, Ren-Rong.
Afiliação
  • Ge FB; College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
  • Lu CJ; College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
  • Chen X; School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
  • Yao W; College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
  • An M; College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
  • Jiang YK; College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
  • Xu LP; School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
  • Liu RR; College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
Angew Chem Int Ed Engl ; 63(26): e202400441, 2024 Jun 21.
Article em En | MEDLINE | ID: mdl-38587149
ABSTRACT
Nickel-catalyzed transannulation reactions triggered by the extrusion of small gaseous molecules have emerged as a powerful strategy for the efficient construction of heterocyclic compounds. However, their use in asymmetric synthesis remains challenging because of the difficulty in controlling stereo- and regioselectivity. Herein, we report the first nickel-catalyzed asymmetric synthesis of N-N atropisomers by the denitrogenative transannulation of benzotriazones with alkynes. A broad range of N-N atropisomers was obtained with excellent regio- and enantioselectivity under mild conditions. Moreover, density functional theory (DFT) calculations provided insights into the nickel-catalyzed reaction mechanism and enantioselectivity control.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China