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An olefin-based multi-component reaction to yield 1,2-azaborolidine derivatives.
Li, Jun; Daniliuc, Constantin G; Kehr, Gerald; Erker, Gerhard.
Afiliación
  • Li J; Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraße 40, 48149, Münster, Germany. erker@uni-muenster.de.
  • Daniliuc CG; Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraße 40, 48149, Münster, Germany. erker@uni-muenster.de.
  • Kehr G; Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraße 40, 48149, Münster, Germany. erker@uni-muenster.de.
  • Erker G; Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstraße 40, 48149, Münster, Germany. erker@uni-muenster.de.
Dalton Trans ; 51(5): 1775-1778, 2022 Feb 01.
Article en En | MEDLINE | ID: mdl-35060579
ABSTRACT
Reaction of the borane FmesBH2·SMe2 [Fmes 2,4,6-tris(trifluoromethyl)phenyl] with two molar equiv. of a small series of 1-alkenes followed by treatment with two molar equivalents of the bulky isonitrile CN-Xyl (Xyl 2,6-dimethylphenyl) gives 1,2-azaborolidine derivatives that exhibit an exocyclic alkene unit and a NHXyl substituent at the heterocyclic core.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Dalton Trans Asunto de la revista: QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Dalton Trans Asunto de la revista: QUIMICA Año: 2022 Tipo del documento: Article País de afiliación: Alemania