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Experimental and Computational Mechanistic Study of Carbonazidate-Initiated Cascade Reactions.
Wang, Qinxuan; Shih, Jiun-Le; Tsui, Ka Yi; Laconsay, Croix J; Tantillo, Dean J; May, Jeremy A.
Afiliación
  • Wang Q; Department of Chemistry, University of Houston, Houston, Texas 77204-5003, United States.
  • Shih JL; Department of Chemistry, University of Houston, Houston, Texas 77204-5003, United States.
  • Tsui KY; Department of Chemistry, University of California─Davis, Davis, California 95616, United States.
  • Laconsay CJ; Department of Chemistry, University of California─Davis, Davis, California 95616, United States.
  • Tantillo DJ; Department of Chemistry, University of California─Davis, Davis, California 95616, United States.
  • May JA; Department of Chemistry, University of Houston, Houston, Texas 77204-5003, United States.
J Org Chem ; 87(14): 8983-9000, 2022 07 15.
Article en En | MEDLINE | ID: mdl-35758036
ABSTRACT
A variety of Huisgen cyclization or nitrene/carbene alkyne cascade reactions with different types of termination were investigated. Accessible nitrene precursors were assessed, and carbonazidates were found to be the only effective initiators. Solvents, terminal alkynyl substituents, and catalysts can all impact the reaction outcome. Study of the mechanism both computationally (by density functional theory) and experimentally revealed relevant intermediates and plausible reaction pathways.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Alquinos Idioma: En Revista: J Org Chem Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Alquinos Idioma: En Revista: J Org Chem Año: 2022 Tipo del documento: Article