Articles producció científica> Química Física i Inorgànica

Reactivity Trends with Borylalkyl Copper(I) Species

  • Identification data

    Identifier: imarina:9219136
    Authors:
    Corro MSalvado OGonzález SDominguez-Molano PFernández E
    Abstract:
    The renaissance on the application of gem-diborylalkanes from 2010, has allowed the conquest of new synthetic application towards C−C and C−N bond formation. The activation of gem-diborylalkanes by Cu(I) catalysts, generates active borylalky copper(I) species that are able to trap several electrophilic reagents, in an efficient way. In addition, the modification of Cu(I) complexes with chiral ligands, induces asymmetric platforms towards the synthesis of enantioenriched organoboron compounds.
  • Others:

    Author, as appears in the article.: Corro M; Salvado O; González S; Dominguez-Molano P; Fernández E
    Department: Química Física i Inorgànica
    URV's Author/s: Corro Morón, Macarena / Domínguez Molano, Paula / Fernández Gutiérrez, Maria Elena / González Morán, Sara / Salvadó Ruiz, Oriol
    Keywords: Α-boryl carbanions Enantioselectivity Electrophilic trapping Diastereoselectivity Copper Alpha-boryl carbanions Allylic substitution olefination gem-diborylalkanes esters enantioselectivity enantioselective synthesis electrophilic trapping diborylmethane diastereoselectivity diastereo copper aldimines aldehydes 1,1-diborylalkanes
    Abstract: The renaissance on the application of gem-diborylalkanes from 2010, has allowed the conquest of new synthetic application towards C−C and C−N bond formation. The activation of gem-diborylalkanes by Cu(I) catalysts, generates active borylalky copper(I) species that are able to trap several electrophilic reagents, in an efficient way. In addition, the modification of Cu(I) complexes with chiral ligands, induces asymmetric platforms towards the synthesis of enantioenriched organoboron compounds.
    Thematic Areas: Química Medicina i Materiais Interdisciplinar Inorganic chemistry Farmacia Engenharias iii Engenharias ii Ciências biológicas ii Ciências biológicas i Chemistry, inorganic & nuclear Astronomia / física
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    Author's mail: oriol.salvado@urv.cat paula.dominguez@urv.cat paula.dominguez@urv.cat sara.gonzalez@urv.cat oriol.salvado@urv.cat mariaelena.fernandez@urv.cat
    Author identifier: 0000-0002-7309-8956 0000-0001-9025-1791
    Record's date: 2024-07-27
    Papper version: info:eu-repo/semantics/publishedVersion
    Link to the original source: https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejic.202100296
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Papper original source: European Journal Of Inorganic Chemistry. 2021 (28): 2802-2813
    APA: Corro M; Salvado O; González S; Dominguez-Molano P; Fernández E (2021). Reactivity Trends with Borylalkyl Copper(I) Species. European Journal Of Inorganic Chemistry, 2021(28), 2802-2813. DOI: 10.1002/ejic.202100296
    Article's DOI: 10.1002/ejic.202100296
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2021
    Publication Type: Journal Publications
  • Keywords:

    Chemistry, Inorganic & Nuclear,Inorganic Chemistry
    Α-boryl carbanions
    Enantioselectivity
    Electrophilic trapping
    Diastereoselectivity
    Copper
    Alpha-boryl carbanions
    Allylic substitution
    olefination
    gem-diborylalkanes
    esters
    enantioselectivity
    enantioselective synthesis
    electrophilic trapping
    diborylmethane
    diastereoselectivity
    diastereo
    copper
    aldimines
    aldehydes
    1,1-diborylalkanes
    Química
    Medicina i
    Materiais
    Interdisciplinar
    Inorganic chemistry
    Farmacia
    Engenharias iii
    Engenharias ii
    Ciências biológicas ii
    Ciências biológicas i
    Chemistry, inorganic & nuclear
    Astronomia / física
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