RT info:eu-repo/semantics/article
T1 Efficient access to polysubstituted tetrahydrofurans by electrophilic cyclization of vinylsilyl alcohols
A1 Barbero Pérez, María Asunción
A1 Barbero San Juan, Héctor
A1 González Ortega, Alfonso
A1 Pulido Pelaz, Francisco José
A1 Val, Patricia
A1 Diez de la Varga, Alberto
A1 Rodríguez Morán, Joaquín
AB Vinylsilyl alcohols undergo intramolecular cyclization to provide di-, tri- or tetrasubstituted-tetrahydrofurans. The influence of the number and position of substituents in the stereoselectivity of the process has been studied. Moreover, DFT calculations have been performed to get better insight into the influence of the substitution pattern of the vinylsilyl alcohol in the stereoselectivity of the cyclization.
PB Royal Society of Chemistry
YR 2015
FD 2015
LK https://uvadoc.uva.es/handle/10324/66278
UL https://uvadoc.uva.es/handle/10324/66278
LA eng
NO RSC Adv., 2015, 5, 49541-49551
NO Producción Científica
DS UVaDOC
RD 22-dic-2024