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Base-controlled dearomative [3 + 2] cycloadditions between 3-nitro-indoles and fumaric acid amide esters.
Tian, Heng-Zhi; Wu, Sheng-Feng; Zhuang, Guo-Wei; Lin, Guo-Qiang; Sun, Xing-Wen.
Afiliación
  • Tian HZ; Department of Chemistry, Fudan University, Shanghai 200433, China. sunxingwen@fudan.edu.cn.
  • Wu SF; Department of Chemistry, Fudan University, Shanghai 200433, China. sunxingwen@fudan.edu.cn.
  • Zhuang GW; Department of Chemistry, Fudan University, Shanghai 200433, China. sunxingwen@fudan.edu.cn.
  • Lin GQ; Department of Chemistry, Fudan University, Shanghai 200433, China. sunxingwen@fudan.edu.cn.
  • Sun XW; Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
Org Biomol Chem ; 20(15): 3072-3075, 2022 04 13.
Article en En | MEDLINE | ID: mdl-35352074
ABSTRACT
The base-controlled dearomative [3 + 2] cycloaddition reaction between 3-nitroindoles and fumaric acid amide esters has been disclosed by using the dearomatization and aromatization strategy. Three kinds of diverse functionalized pyrrolo[2,3-b]indole derivatives were obtained respectively with excellent chemoselectivities and good diastereoselectivities using different bases.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Amidas / Indoles Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Amidas / Indoles Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: China