Organocatalytic functionalisation through boron chemistry

Gerard Palau-Lluch; Xavier Sanz; Enrico La Cascia; Marc G. Civit; Nuria Miralles; Ana B. Cuenca; Elena Fernández

doi:10.1515/pac-2014-0934

Organocatalytic functionalisation through boron chemistry

Gerard Palau-Lluch, Xavier Sanz, Enrico La Cascia, Marc G. Civit, Nuria Miralles, Ana B. Cuenca, Elena Fernández^*

^*Autor/a de correspondencia de este trabajo

Producción científica: Artículo en revista indizada › Artículo › revisión exhaustiva

10 Citas (Scopus)

Resumen

Diboron reagents can be activated both, from a metal or free-metal context, and consequently the addition of boryl units to unsaturated substrates proceeds sometimes with complementary selectivity. We highlight here the power of boron chemistry to functionalize molecules and provide new routes towards challenging compounds.

Idioma original	Inglés
Páginas (desde-hasta)	181-193
Número de páginas	13
Publicación	Pure and Applied Chemistry
Volumen	87
N.º	2
DOI	https://doi.org/10.1515/pac-2014-0934
Estado	Publicada - 1 feb 2015
Publicado de forma externa	Sí
Evento	15th International Conference on Boron Chemistry (IMEBORON) - Prague, República Checa Duración: 24 ago 2014 → 28 ago 2014

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title = "Organocatalytic functionalisation through boron chemistry",

abstract = "Diboron reagents can be activated both, from a metal or free-metal context, and consequently the addition of boryl units to unsaturated substrates proceeds sometimes with complementary selectivity. We highlight here the power of boron chemistry to functionalize molecules and provide new routes towards challenging compounds.",

keywords = "Boranes, Enantioselectivity, IMEBORON XV, Nucleophilic addition",

author = "Gerard Palau-Lluch and Xavier Sanz and {La Cascia}, Enrico and Civit, {Marc G.} and Nuria Miralles and Cuenca, {Ana B.} and Elena Fern{\'a}ndez",

note = "Publisher Copyright: {\textcopyright} 2014 IUPAC & De Gruyter.; 15th International Conference on Boron Chemistry (IMEBORON) ; Conference date: 24-08-2014 Through 28-08-2014",

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AU - Palau-Lluch, Gerard

AU - Sanz, Xavier

AU - La Cascia, Enrico

AU - Civit, Marc G.

AU - Miralles, Nuria

AU - Cuenca, Ana B.

AU - Fernández, Elena

PY - 2015/2/1

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N2 - Diboron reagents can be activated both, from a metal or free-metal context, and consequently the addition of boryl units to unsaturated substrates proceeds sometimes with complementary selectivity. We highlight here the power of boron chemistry to functionalize molecules and provide new routes towards challenging compounds.

AB - Diboron reagents can be activated both, from a metal or free-metal context, and consequently the addition of boryl units to unsaturated substrates proceeds sometimes with complementary selectivity. We highlight here the power of boron chemistry to functionalize molecules and provide new routes towards challenging compounds.

KW - Boranes

KW - Enantioselectivity

KW - IMEBORON XV

KW - Nucleophilic addition

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T2 - 15th International Conference on Boron Chemistry (IMEBORON)

Y2 - 24 August 2014 through 28 August 2014

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Organocatalytic functionalisation through boron chemistry

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