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Organocatalytic Strategies for the Development of the Enantioselective Inverse-electron-demand Hetero-Diels-Alder Reaction.
Laina-Martín, Víctor; Fernández-Salas, Jose A; Alemán, José.
Afiliación
  • Laina-Martín V; Departamento de Química Orgánica (módulo 1) Facultad de Ciencias, Universidad Autónoma de Madrid, 28049-, Madrid, Spain.
  • Fernández-Salas JA; Departamento de Química Orgánica (módulo 1) Facultad de Ciencias, Universidad Autónoma de Madrid, 28049-, Madrid, Spain.
  • Alemán J; Institute for Advanced Research in Chemical Sciences (IAdChem), Universidad Autónoma de Madrid, 28049-, Madrid, Spain.
Chemistry ; 27(49): 12509-12520, 2021 Sep 01.
Article en En | MEDLINE | ID: mdl-34132427
ABSTRACT
Cycloaddition reactions, in particular Diels-Alder reactions, have attracted a lot of attention from organic chemists since they represent one of the most powerful methodologies for the construction of carbon-carbon bonds. In particular, inverse-electron-demand hetero-Diels-Alder reactions have been an important breakthrough for the synthesis of heterocyclic compounds. Among all their variants, the organocatalytic enantioselective version has been widely explored since the asymmetric construction of diversely functionalized scaffolds under reaction conditions encompassed within the green chemistry field is of great interest. In this review, a profound revision on the latest advances on the organocatalytic asymmetric inverse-electron demand hetero-Diels-Alder reaction is shown.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Electrones / Compuestos Heterocíclicos Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Electrones / Compuestos Heterocíclicos Idioma: En Revista: Chemistry Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: España