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Iodobenzene-Catalyzed Ortho-Dearomatization and Aromatization-Triggered Rearrangement of 2-Allylanilines: Construction of Indolin-3-ylmethanols with High Diastereoselectivities.
Wang, Shuo-En; He, Qiuqin; Fan, Renhua.
Afiliación
  • Wang SE; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, China.
  • He Q; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, China.
  • Fan R; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, China.
Org Lett ; 19(24): 6478-6481, 2017 12 15.
Article en En | MEDLINE | ID: mdl-29192793
An iodobenzene-catalyzed oxidative rearrangement of 2-allylanilines was developed. This process involves an ortho-oxidative dearomatization mediated by the in situ generated iodine(III) compound and a subsequent aromatization-triggered rearrangement reaction, leading to the formation of functionalized indolin-3-ylmethanols with high diastereoselectivities.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2017 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2017 Tipo del documento: Article País de afiliación: China
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