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C-H alkenylation/cyclization and sulfamidation of 2-phenylisatogens using N-oxide as a directing group.
Guo, Lingmei; Tang, Baolan; Nie, Ruifang; Liu, Yanzhao; Lv, Shan; Wang, Huijing; Guo, Li; Hai, Li; Wu, Yong.
Afiliación
  • Guo L; Key Laboratory of Drug Targeting and Drug Delivery System of Education Ministry, Department of Medicinal Chemistry, West China School of Pharmacy, Sichuan University, No. 17, 3th Section, South Renmin Road, Chengdu, 610041, P. R. China. smile@scu.edu.cn wyong@scu.edu.cn.
Chem Commun (Camb) ; 55(71): 10623-10626, 2019 Aug 29.
Article en En | MEDLINE | ID: mdl-31429452
ABSTRACT
The first example of transition-metal-catalyzed C-H activations of 2-phenylisatogens with alkynes and sulfonyl azides has been developed using N-oxide as the directing group. Ru(ii)-Catalyzed C-H alkenylation/cyclization and Ir(iii)-catalyzed direct C-H sulfamidation proceeded with good yields and excellent functional group tolerance. Importantly, these two transformations provided straightforward routes for the synthesis of indol-3-one derivatives and sulfamidated 2-phenylisatogens respectively, which might be of considerable bioactivities.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Chem Commun (Camb) Asunto de la revista: QUIMICA Año: 2019 Tipo del documento: Article