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Access to Piperazine-Fused Pyrrolocarbazoles Enabled by Acid-Catalyzed Stereoselective Hydroarylation of Ynamide-Indoles and Subsequent Diels-Alder Reactions/Aromatizations.
Zhou, Ze; Huang, Xiang; Wei, Qing-Yi; Wang, Yi-Lin; Wu, Bin; Yang, Jin-Ming.
Afiliación
  • Zhou Z; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China.
  • Huang X; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China.
  • Wei QY; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China.
  • Wang YL; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China.
  • Wu B; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China.
  • Yang JM; School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan 430074, People's Republic of China.
Org Lett ; 26(35): 7273-7278, 2024 Sep 06.
Article en En | MEDLINE | ID: mdl-39133635
ABSTRACT
Pyrrolocarbazole skeletons are well known to possess a variety of biological activities that might be therapeutically useful in the treatment of cancers. Herein, an acid-catalyzed stereoselective hydroarylation/Diels-Alder cycloaddition/aromatization of ynamide-indoles is described. We newly designed and synthesized a variety of piperazine-fused pyrrolocarbazole derivatives that could be further applied to the synthesis of potent Wee1 inhibitors.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos