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Photocatalytic Bicyclization of Indole-Tethered 1,6-Enynes for Diastereoselective Synthesis of Pyrrolo[3,2,1-jk]carbazoles.
Zuo, Hang-Dong; Chen, Xi; Yuan, Ya-Yu; Zhang, Yue; Liu, Jian-Wu; Yan, Sheng-Hu; Hao, Wen-Juan; Jiang, Bo.
Afiliação
  • Zuo HD; Continuous Flow Engineering Laboratory of National Petroleum and Chemical Industry, Changzhou University, Changzhou, Jiangsu 213164, China.
  • Chen X; School of Safety Science and Engineering, Changzhou University, Changzhou, Jiangsu 213164, China.
  • Yuan YY; Continuous Flow Engineering Laboratory of National Petroleum and Chemical Industry, Changzhou University, Changzhou, Jiangsu 213164, China.
  • Zhang Y; School of Pharmacy, Changzhou University, Changzhou, Jiangsu 213164, China.
  • Liu JW; Continuous Flow Engineering Laboratory of National Petroleum and Chemical Industry, Changzhou University, Changzhou, Jiangsu 213164, China.
  • Yan SH; School of Pharmacy, Changzhou University, Changzhou, Jiangsu 213164, China.
  • Hao WJ; Continuous Flow Engineering Laboratory of National Petroleum and Chemical Industry, Changzhou University, Changzhou, Jiangsu 213164, China.
  • Jiang B; School of Pharmacy, Changzhou University, Changzhou, Jiangsu 213164, China.
Org Lett ; 26(18): 3810-3815, 2024 May 10.
Article em En | MEDLINE | ID: mdl-38678579
ABSTRACT
A visible-light-driven photocatalytic protocol is established for the diastereoselective synthesis of pyrrolo[3,2,1-jk]carbazoles via a radical-triggered multicomponent bicyclization reaction starting from readily available indole-tethered 1,6-enynes and α-benzyl-α-bromomalonates under mild conditions. This photocatalytic approach exhibits a wide substrate compatibility and excellent tolerability toward various functional groups and boasts the benefit of efficient ring formation and chemical bond creation.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China