Articles producció científica> Química Física i Inorgànica

Boron-Wittig olefination with: Gem -bis(boryl)alkanes

  • Dades identificatives

    Identificador: imarina:9150156
    Autors:
    Cuenca ABFernández E
    Resum:
    © The Royal Society of Chemistry. The condensation of easy manageable lithium α-bis(boryl)carbanions with carbonyl derivatives, the so-called boron-Wittig reaction, allows for the straightforward and often stereoselective formation of synthetically highly versatile metalloid-substituted alkenes, which are key building blocks on route to all-carbon substituted olefins. In this Tutorial review the concept behind this olefination reaction and its application to ketones, aldehydes and other carbonyl derivatives, such amides, ester and carboxylic acids, are presented in a systematic manner. A special emphasis has been placed on parameters controlling the stereochemical outcome of these transformations. To illustrate the great synthetic potential of this new methodological tool, a section is also included covering a selection of applications of the boron-Wittig reaction to target compounds via subsequent C-C bond-forming process. This journal is
  • Altres:

    Autor segons l'article: Cuenca AB; Fernández E
    Departament: Química Física i Inorgànica
    e-ISSN: 1460-4744
    Autor/s de la URV: Fernández Gutiérrez, Maria Elena
    Paraules clau: Stereoselective-synthesis Ketones Generation Esters Deprotonation Carbonyl-compounds Carbanions Bis(ethylenedioxyboryl)methide Aldehydes
    Resum: © The Royal Society of Chemistry. The condensation of easy manageable lithium α-bis(boryl)carbanions with carbonyl derivatives, the so-called boron-Wittig reaction, allows for the straightforward and often stereoselective formation of synthetically highly versatile metalloid-substituted alkenes, which are key building blocks on route to all-carbon substituted olefins. In this Tutorial review the concept behind this olefination reaction and its application to ketones, aldehydes and other carbonyl derivatives, such amides, ester and carboxylic acids, are presented in a systematic manner. A special emphasis has been placed on parameters controlling the stereochemical outcome of these transformations. To illustrate the great synthetic potential of this new methodological tool, a section is also included covering a selection of applications of the boron-Wittig reaction to target compounds via subsequent C-C bond-forming process. This journal is
    Àrees temàtiques: Química Materiais General medicine General chemistry Ciências biológicas ii Ciência de alimentos Chemistry, multidisciplinary Chemistry (miscellaneous) Chemistry (all) Chemistry Antropologia / arqueologia
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 0306-0012
    Adreça de correu electrònic de l'autor: mariaelena.fernandez@urv.cat
    Identificador de l'autor: 0000-0001-9025-1791
    Data d'alta del registre: 2024-07-27
    Versió de l'article dipositat: info:eu-repo/semantics/acceptedVersion
    Enllaç font original: https://pubs.rsc.org/en/content/articlelanding/2021/cs/d0cs00953a#!divAbstract
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Chemical Society Reviews. 50 (1): 72-86
    Referència de l'ítem segons les normes APA: Cuenca AB; Fernández E (2021). Boron-Wittig olefination with: Gem -bis(boryl)alkanes. Chemical Society Reviews, 50(1), 72-86. DOI: 10.1039/d0cs00953a
    DOI de l'article: 10.1039/d0cs00953a
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2021
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Chemistry,Chemistry (Miscellaneous),Chemistry, Multidisciplinary
    Stereoselective-synthesis
    Ketones
    Generation
    Esters
    Deprotonation
    Carbonyl-compounds
    Carbanions
    Bis(ethylenedioxyboryl)methide
    Aldehydes
    Química
    Materiais
    General medicine
    General chemistry
    Ciências biológicas ii
    Ciência de alimentos
    Chemistry, multidisciplinary
    Chemistry (miscellaneous)
    Chemistry (all)
    Chemistry
    Antropologia / arqueologia
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