Articles producció científica> Química Física i Inorgànica

Selective C-C coupling of vinyl epoxides with diborylmethide lithium salts

  • Datos identificativos

    Identificador: imarina:5133299
    Autores:
    Gava, RiccardoFernandez, Elena
    Resumen:
    © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Vinyl epoxides and styrene oxide can react with diborylmethide lithium salts through an exclusive SN2 borylmethylation/ring opening in a regio- and diastereoselective way, depending on the nature of the substrate. The ring-opening protocol provides homoallylboronates that can be transformed into challenging diastereomeric bishomoallylic alicyclic 1,3-diols. Unprecedented 3-borylated 1,2-oxaborolan-2-ol products were prepared by borylmethylation/ring opening of 2-methyl-2-vinyloxirane followed by intramolecular cyclization.
  • Otros:

    Autor según el artículo: Gava, Riccardo; Fernandez, Elena
    Departamento: Química Física i Inorgànica
    Autor/es de la URV: Fernández Gutiérrez, Maria Elena
    Palabras clave: S(n)2 mechanism S 2 mechanism n Lithium salts Ketones Insertion Homoallylboronates Geminal diborylalkanes Gem-silylborylation Esters Diborylalkanes Diboronates Deprotonation Carbanions Alkyl-halides Aldehydes Access sn2 mechanism homoallylboronates geminal diborylalkanes diboronates
    Resumen: © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Vinyl epoxides and styrene oxide can react with diborylmethide lithium salts through an exclusive SN2 borylmethylation/ring opening in a regio- and diastereoselective way, depending on the nature of the substrate. The ring-opening protocol provides homoallylboronates that can be transformed into challenging diastereomeric bishomoallylic alicyclic 1,3-diols. Unprecedented 3-borylated 1,2-oxaborolan-2-ol products were prepared by borylmethylation/ring opening of 2-methyl-2-vinyloxirane followed by intramolecular cyclization.
    Áreas temáticas: Química Organic chemistry Medicina i Materiais Interdisciplinar General medicine General chemistry Farmacia Engenharias iii Engenharias ii Ciências biológicas iii Ciências biológicas ii Ciências biológicas i Ciências agrárias i Chemistry, multidisciplinary Chemistry (miscellaneous) Chemistry (all) Chemistry Catalysis Biotecnología Biodiversidade Astronomia / física
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 15213765
    Direcció de correo del autor: mariaelena.fernandez@urv.cat
    Identificador del autor: 0000-0001-9025-1791
    Fecha de alta del registro: 2023-07-31
    Versión del articulo depositado: info:eu-repo/semantics/acceptedVersion
    Referencia al articulo segun fuente origial: Chemistry-A European Journal. 25 (34): 8013-8017
    Referencia de l'ítem segons les normes APA: Gava, Riccardo; Fernandez, Elena (2019). Selective C-C coupling of vinyl epoxides with diborylmethide lithium salts. Chemistry-A European Journal, 25(34), 8013-8017. DOI: 10.1002/chem.201901406
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2019
    Tipo de publicación: Journal Publications
  • Palabras clave:

    Catalysis,Chemistry,Chemistry (Miscellaneous),Chemistry, Multidisciplinary,Organic Chemistry
    S(n)2 mechanism
    S 2 mechanism n
    Lithium salts
    Ketones
    Insertion
    Homoallylboronates
    Geminal diborylalkanes
    Gem-silylborylation
    Esters
    Diborylalkanes
    Diboronates
    Deprotonation
    Carbanions
    Alkyl-halides
    Aldehydes
    Access
    sn2 mechanism
    homoallylboronates
    geminal diborylalkanes
    diboronates
    Química
    Organic chemistry
    Medicina i
    Materiais
    Interdisciplinar
    General medicine
    General chemistry
    Farmacia
    Engenharias iii
    Engenharias ii
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Ciências agrárias i
    Chemistry, multidisciplinary
    Chemistry (miscellaneous)
    Chemistry (all)
    Chemistry
    Catalysis
    Biotecnología
    Biodiversidade
    Astronomia / física
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