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CF2Br2 as a Source for Difluoroolefination of 1,3-Enynes via N-Heterocyclic Carbene Catalysis.
Chen, Lei; Wang, Jingyi; Lin, Chen; Zhu, Yiwei; Du, Ding.
Afiliación
  • Chen L; State Key Laboratory of Natural Medicines, School of Science, China Pharmaceutical University, Nanjing, 210009, P.R. China.
  • Wang J; State Key Laboratory of Natural Medicines, School of Science, China Pharmaceutical University, Nanjing, 210009, P.R. China.
  • Lin C; State Key Laboratory of Natural Medicines, School of Science, China Pharmaceutical University, Nanjing, 210009, P.R. China.
  • Zhu Y; School of Chemistry and Environmental Engineering, Anhui Polytechnic University, Wuhu, Anhui 241000, P.R. China.
  • Du D; State Key Laboratory of Natural Medicines, School of Science, China Pharmaceutical University, Nanjing, 210009, P.R. China.
Org Lett ; 24(38): 7047-7051, 2022 Sep 30.
Article en En | MEDLINE | ID: mdl-36121666
Commercially available CF2Br2 has been used as a convenient source for the rapid and reliable incorporation of the gem-difluorovinyl motif into an allene framework via an N-heterocyclic carbene catalyzed difluoroolefination of 1,3-enynes. The reaction proceeds through a cascade three-component radical relay/elimination process. This protocol is distinguished by its mild conditions, readily accessible starting materials, wide substrate scope, and ease of late-stage functionalization, thus unlocking an untraditional strategy to construct a new class of functionalized gem-difluorovinyl allenes.

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 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: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos