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Cascade hydroarylation/Diels-Alder cycloaddition of alkynylindoles with electron-deficient alkynes and alkenes.
Feng, Guang-Chao; Li, Jun-Chi; Huang, Xiang; Liu, Ji-Kai; Wu, Bin; Yang, Jin-Ming.
Afiliación
  • Feng GC; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China. jmyang@scuec.edu.cn.
  • Li JC; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China. jmyang@scuec.edu.cn.
  • Huang X; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China. jmyang@scuec.edu.cn.
  • Liu JK; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China. jmyang@scuec.edu.cn.
  • Wu B; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China. jmyang@scuec.edu.cn.
  • Yang JM; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China. jmyang@scuec.edu.cn.
Chem Commun (Camb) ; 60(3): 328-331, 2024 Jan 02.
Article en En | MEDLINE | ID: mdl-38063477
ABSTRACT
Herein, a novel cascade gold(I)-catalyzed hydroarylation of alkynylindoles and subsequent Diels-Alder cycloaddition with electron-deficient alkynes and alkenes is described. A variety of azepino-fused hydrocarbazoles and carbazoles were obtained in moderate to excellent yields. Key features of this methodology are low catalyst loadings, high regioselectivity, broad functional group tolerances, access to important heterocycles, and 100% atom economy.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article