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Photoredox and Copper Dual-Catalyzed Cyclization of Alkyne-tethered α-Bromocarbonyls.
Wang, Zi-Ying; Cai, Xue-Er; Zhang, Can-Can; Yang, Wen-Hui; Wang, Ling-Tao; Xu, Qing; Liu, Hongxin; Wei, Wen-Ting.
Afiliação
  • Wang ZY; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
  • Cai XE; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
  • Zhang CC; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
  • Yang WH; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
  • Wang LT; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
  • Xu Q; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
  • Liu H; College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang, 325035, China.
  • Wei WT; School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211, China.
Chem Asian J ; 18(18): e202300606, 2023 Sep 15.
Article em En | MEDLINE | ID: mdl-37500593
ABSTRACT
The synergistic systems of photoredox and copper catalyst have already appeared as a novel formation of green synthetic chemistry, which open new avenues for chemical synthesis applications. We describe a novel strategy for the cyclization of alkyne-tethered α-bromocarbonyls initiated by the cleavage of C(sp3 )-Br bond via the collaboration of photoredox and copper catalyst. The present protocol exhibits mildness using economical copper catalyst and visible-light at room temperature. The gram-scale and sunlight irradiation experiments proceeded smoothly to show the practicality of the methodology. It is notable that the newly generated oxygen in the product originates from H2 O.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Chem Asian J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Chem Asian J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China