Articles producció científicaQuímica Física i Inorgànica

Tri(boryl)alkanes and tri(boryl)alkenes: The versatile reagents

  • Dades identificatives

    Identificador:  imarina:6238580
    Autors:  Salvado, Oriol; Fernandez, Elena
    Resum:
    © 2020 by the authors. The interest of organoboron chemistry in organic synthesis is growing, together with the development of new and versatile polyborated reagents. Here, the preparation of 1,1,1-tri(boryl)alkanes, 1,2,3-tri(boryl)alkanes, 1,1,2-tri(boryl)alkanes, as well as 1,1,2-tri(boryl)alkenes as suitable and accessible polyborated systems is demonstrated as being easily applied in the construction of new carbon-carbon and carbon-heteroatom bonds. Synthetic procedures and limitations have been collected to demonstrate the powerful strategies to construct selective molecules, taking advantages of the easy transformation of carbon-boron bond in multiple functionalities, under the total control of chemo- and stereoselectivity.
  • Altres:

    Autor segons l'article: Salvado, Oriol; Fernandez, Elena
    Departament: Química Física i Inorgànica
    Autor/s de la URV: Fernández Gutiérrez, Maria Elena / Fernández López, Elena / Salvadó Ruiz, Oriol
    Paraules clau: Terminal alkynes; Synthetic approaches; Synthetic applications; Stereoisomerism; Models, chemical; Ketones; Esters; Diboration; Construction; Chemistry techniques, synthetic; Borylation; Alkylation; Alkenes; Aldehydes; 1,2,3-tri(boryl)alkanes; 1,1,2-tri(boryl)alkenes; 1,1,2-tri(boryl)alkanes; 1,1,2-tri(boryl) alkenes; 1,1,1-tri(boryl)alkanes; synthetic applications; 1,2,3-tri(boryl)alkanes; 1,1,2-tri(boryl)alkenes; 1,1,2-tri(boryl)alkanes; 1,1,1-tri(boryl)alkanes
    Resum: © 2020 by the authors. The interest of organoboron chemistry in organic synthesis is growing, together with the development of new and versatile polyborated reagents. Here, the preparation of 1,1,1-tri(boryl)alkanes, 1,2,3-tri(boryl)alkanes, 1,1,2-tri(boryl)alkanes, as well as 1,1,2-tri(boryl)alkenes as suitable and accessible polyborated systems is demonstrated as being easily applied in the construction of new carbon-carbon and carbon-heteroatom bonds. Synthetic procedures and limitations have been collected to demonstrate the powerful strategies to construct selective molecules, taking advantages of the easy transformation of carbon-boron bond in multiple functionalities, under the total control of chemo- and stereoselectivity.
    Àrees temàtiques: Zootecnia / recursos pesqueiros; Saúde coletiva; Química; Psicología; Planejamento urbano e regional / demografia; Physical and theoretical chemistry; Pharmaceutical science; Organic chemistry; Odontología; Nutrição; Molecular medicine; Medicine (miscellaneous); Medicina veterinaria; Medicina iii; Medicina ii; Medicina i; Materiais; Matemática / probabilidade e estatística; Interdisciplinar; Geografía; General medicine; Farmacia; Ensino; Engenharias iv; Engenharias iii; Engenharias ii; Engenharias i; Educação física; Economia; Drug discovery; Ciências biológicas iii; Ciências biológicas ii; Ciências biológicas i; Ciências ambientais; Ciências agrárias i; Ciência de alimentos; Ciência da computação; Chemistry, organic; Chemistry, multidisciplinary; Chemistry (miscellaneous); Biotecnología; Biodiversidade; Biochemistry & molecular biology; Astronomia / física; Analytical chemistry
    Accès a la llicència d'ús: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 14203049
    Adreça de correu electrònic de l'autor: oriol.salvado@alumni.urv.cat; mariaelena.fernandez@urv.cat
    Data d'alta del registre: 2025-02-18
    Versió de l'article dipositat: info:eu-repo/semantics/publishedVersion
    Enllaç font original: https://www.mdpi.com/1420-3049/25/7/1758
    URL Document de llicència: https://repositori.urv.cat/ca/proteccio-de-dades/
    Referència a l'article segons font original: Molecules. 25 (7): 1758-
    Referència de l'ítem segons les normes APA: Salvado, Oriol; Fernandez, Elena (2020). Tri(boryl)alkanes and tri(boryl)alkenes: The versatile reagents. Molecules, 25(7), 1758-. DOI: 10.3390/molecules25071758
    DOI de l'article: 10.3390/molecules25071758
    Entitat: Universitat Rovira i Virgili
    Any de publicació de la revista: 2020
    Tipus de publicació: Journal Publications
  • Paraules clau:

    Analytical Chemistry,Biochemistry & Molecular Biology,Chemistry (Miscellaneous),Chemistry, Multidisciplinary,Chemistry, Organic,Drug Discovery,Medicine (Miscellaneous),Molecular Medicine,Organic Chemistry,Pharmaceutical Science,Physical and Theoretical Chemistry
    Terminal alkynes
    Synthetic approaches
    Synthetic applications
    Stereoisomerism
    Models, chemical
    Ketones
    Esters
    Diboration
    Construction
    Chemistry techniques, synthetic
    Borylation
    Alkylation
    Alkenes
    Aldehydes
    1,2,3-tri(boryl)alkanes
    1,1,2-tri(boryl)alkenes
    1,1,2-tri(boryl)alkanes
    1,1,2-tri(boryl) alkenes
    1,1,1-tri(boryl)alkanes
    synthetic applications
    1,2,3-tri(boryl)alkanes
    1,1,2-tri(boryl)alkenes
    1,1,2-tri(boryl)alkanes
    1,1,1-tri(boryl)alkanes
    Zootecnia / recursos pesqueiros
    Saúde coletiva
    Química
    Psicología
    Planejamento urbano e regional / demografia
    Physical and theoretical chemistry
    Pharmaceutical science
    Organic chemistry
    Odontología
    Nutrição
    Molecular medicine
    Medicine (miscellaneous)
    Medicina veterinaria
    Medicina iii
    Medicina ii
    Medicina i
    Materiais
    Matemática / probabilidade e estatística
    Interdisciplinar
    Geografía
    General medicine
    Farmacia
    Ensino
    Engenharias iv
    Engenharias iii
    Engenharias ii
    Engenharias i
    Educação física
    Economia
    Drug discovery
    Ciências biológicas iii
    Ciências biológicas ii
    Ciências biológicas i
    Ciências ambientais
    Ciências agrárias i
    Ciência de alimentos
    Ciência da computação
    Chemistry, organic
    Chemistry, multidisciplinary
    Chemistry (miscellaneous)
    Biotecnología
    Biodiversidade
    Biochemistry & molecular biology
    Astronomia / física
    Analytical chemistry
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