Articles producció científica> Química Física i Inorgànica

α-Boryl Carbanions: The Influence of Geminal Heteroatoms in C-C Bond Formation

  • Identification data

    Identifier: imarina:9440133
    Authors:
    Fernandez, Elena
    Abstract:
    The wide applications of alpha-boryl carbanions in selective coupling with organohalides, imines/carbonyls and conjugated unsaturated substrates has become an interesting tool for organic synthesis. Strategically, the inclusion of heteroatoms, such as Si, S, N, F, Cl, Br and I in the alpha position opens a new venue towards multifunctionalities in molecular design. Here, a conceptual and practical view on powerful carbanions, containing alpha-silicoboron, alpha-thioboron, alpha-haloboron and alpha-aminoboron is given, as well as a prespective on their efficient application for selective electrophilic trapping.
  • Others:

    Author, as appears in the article.: Fernandez, Elena
    Department: Química Física i Inorgànica
    URV's Author/s: Fernández Gutiérrez, Maria Elena
    Keywords: Allylic substitution Alpha-aminoboron carbanion Alpha-boryl carbanion Alpha-haloboron carbanio Alpha-silicoboron carbanion Alpha-thioboron carbanion Asymmetric-synthesis Boronic esters Carbonyl-compounds Catalyzed diborylation Diborylmethan Enantioselective synthesis Gem-diborylalkanes Metal-free synthesis Stereoselective-synthesis Α-aminoboron carbanion Α-boryl carbanion Α-haloboron carbanion Α-silicoboron carbanion Α-thioboron carbanion
    Abstract: The wide applications of alpha-boryl carbanions in selective coupling with organohalides, imines/carbonyls and conjugated unsaturated substrates has become an interesting tool for organic synthesis. Strategically, the inclusion of heteroatoms, such as Si, S, N, F, Cl, Br and I in the alpha position opens a new venue towards multifunctionalities in molecular design. Here, a conceptual and practical view on powerful carbanions, containing alpha-silicoboron, alpha-thioboron, alpha-haloboron and alpha-aminoboron is given, as well as a prespective on their efficient application for selective electrophilic trapping.
    Thematic Areas: Biochemistry Biochemistry (medical) Chemical engineering (all) Chemical engineering (miscellaneous) Chemistry (all) Chemistry (miscellaneous) Chemistry, multidisciplinary Ciência de alimentos Engenharias ii General chemical engineering General chemistry Materials chemistry Medicine (miscellaneous)
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    Author's mail: mariaelena.fernandez@urv.cat
    Author identifier: 0000-0001-9025-1791
    Record's date: 2025-02-18
    Paper version: info:eu-repo/semantics/publishedVersion
    Paper original source: Chemical Record. 24 (3): e202300349-
    APA: Fernandez, Elena (2024). α-Boryl Carbanions: The Influence of Geminal Heteroatoms in C-C Bond Formation. Chemical Record, 24(3), e202300349-. DOI: 10.1002/tcr.202300349
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2024
    Publication Type: Journal Publications
  • Keywords:

    Biochemistry,Biochemistry (Medical),Chemical Engineering (Miscellaneous),Chemistry (Miscellaneous),Chemistry, Multidisciplinary,Materials Chemistry,Medicine (Miscellaneous)
    Allylic substitution
    Alpha-aminoboron carbanion
    Alpha-boryl carbanion
    Alpha-haloboron carbanio
    Alpha-silicoboron carbanion
    Alpha-thioboron carbanion
    Asymmetric-synthesis
    Boronic esters
    Carbonyl-compounds
    Catalyzed diborylation
    Diborylmethan
    Enantioselective synthesis
    Gem-diborylalkanes
    Metal-free synthesis
    Stereoselective-synthesis
    Α-aminoboron carbanion
    Α-boryl carbanion
    Α-haloboron carbanion
    Α-silicoboron carbanion
    Α-thioboron carbanion
    Biochemistry
    Biochemistry (medical)
    Chemical engineering (all)
    Chemical engineering (miscellaneous)
    Chemistry (all)
    Chemistry (miscellaneous)
    Chemistry, multidisciplinary
    Ciência de alimentos
    Engenharias ii
    General chemical engineering
    General chemistry
    Materials chemistry
    Medicine (miscellaneous)
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