Articles producció científicaQuímica Física i Inorgànica

Opportune gem-silylborylation of carbonyl compounds: a modular and stereocontrolled entry to tetrasubstituted olefins

  • Dades identificatives

    Identificador:  imarina:3658141
    Autors:  La Cascia, Enrico; Cuenca, Ana B; Fernandez, Elena
    Resum:
    An easy access to highly versatile gem-silylboro-nate synthons is achieved by means of an new olefination reagent, HC(B pin)2(SiMe3). Subsequent silicon or boron-based selective functionalization allows for the modular and stereocontrolled synthesis of all-carbon tetrasubstitut-ed alkenes.Aparticular attraction of this approach is the iodode silylation reaction, whichbecomes apivotaltool for C-Si functionalization.
  • Altres:

    Autor segons l'article: La Cascia, Enrico; Cuenca, Ana B; Fernandez, Elena
    Departament: Química Física i Inorgànica
    Autor/s de la URV: Fernández Gutiérrez, Maria Elena
    Paraules clau: Tamoxifen; Iododesilylation; Insertion; Gem-silylborylation; Alkenes; iododesilylation; insertion; gem-silylborylation; alkenes
    Resum: An easy access to highly versatile gem-silylboro-nate synthons is achieved by means of an new olefination reagent, HC(B pin)2(SiMe3). Subsequent silicon or boron-based selective functionalization allows for the modular and stereocontrolled synthesis of all-carbon tetrasubstitut-ed alkenes.Aparticular attraction of this approach is the iodode silylation reaction, whichbecomes apivotaltool for C-Si functionalization.
    Àrees temàtiques: 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
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    Adreça de correu electrònic de l'autor: mariaelena.fernandez@urv.cat
    Data d'alta del registre: 2025-02-18
    Versió de l'article dipositat: info:eu-repo/semantics/acceptedVersion
    Enllaç font original: https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.201604782
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Chemistry-A European Journal. 22 (52): 18737-18741
    Referència de l'ítem segons les normes APA: La Cascia, Enrico; Cuenca, Ana B; Fernandez, Elena (2016). Opportune gem-silylborylation of carbonyl compounds: a modular and stereocontrolled entry to tetrasubstituted olefins. Chemistry-A European Journal, 22(52), 18737-18741. DOI: 10.1002/chem.201604782
    DOI de l'article: 10.1002/chem.201604782
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2016
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Catalysis,Chemistry,Chemistry (Miscellaneous),Chemistry, Multidisciplinary,Organic Chemistry
    Tamoxifen
    Iododesilylation
    Insertion
    Gem-silylborylation
    Alkenes
    iododesilylation
    insertion
    gem-silylborylation
    alkenes
    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
  • Documents:

  • Cerca a google

    Search to google scholar