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Regiocontrolled Annulation of Benzocyclobutenols with Alkynes.
Zeng, Qin-Qiong; Wang, Yong-Qi; Cheng, Lang; Wang, Bi-Qin; Hu, Ping; Song, Feijie.
Afiliación
  • Zeng QQ; College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066, P. R. China.
  • Wang YQ; College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066, P. R. China.
  • Cheng L; College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066, P. R. China.
  • Wang BQ; College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066, P. R. China.
  • Hu P; College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066, P. R. China.
  • Song F; College of Chemistry and Materials Science, Sichuan Normal University, Chengdu, Sichuan 610066, P. R. China.
Org Lett ; 24(16): 3058-3063, 2022 Apr 29.
Article en En | MEDLINE | ID: mdl-35426691
ABSTRACT
A tandem reaction that involves an unprecedented Rh-catalyzed intramolecular annulation of benzocyclobutenols with alkynes and subsequent ZnCl2-promoted dehydration was developed, offering an efficient approach to 2H-furan-, pyran-, and oxepine-fused naphthalenes. Furthermore, the 2H-furan motif may undergo a ring-opening reaction through Fe-catalyzed reductive C-O bond cleavage. As a consequence, the formal intermolecular annulation of 2-hydroxybenzocyclobutenols with alkynes was realized with complete regioselectivity through a two-step protocol.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2022 Tipo del documento: Article
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