ChemInform Abstract: Efficient Access to Polysubstituted Tetrahydrofurans by Electrophilic Cyclization of Vinylsilyl Alcohols.

  1. Barbero, Asuncion 1
  2. Barbero, Hector 1
  3. Gonzalez-Ortega, Alfonso 1
  4. Pulido, Francisco J. 1
  5. Val, Patricia 1
  6. Diez-Varga, Alberto 1
  7. Moran, Joaquin R. 1
  1. 1 Universidad de Valladolid
    info

    Universidad de Valladolid

    Valladolid, España

    ROR https://ror.org/01fvbaw18

Revue:
ChemInform

ISSN: 0931-7597

Année de publication: 2015

Volumen: 46

Número: 41

Pages: no-no

Type: Article

DOI: 10.1002/CHIN.201541121 GOOGLE SCHOLAR lock_openAccès ouvert editor

D'autres publications dans: ChemInform

Résumé

Vinylsilyl alcohols undergo intramolecular cyclization toprovide di-, tri- or tetrasubstituted-tetrahydrofurans. The influence of the number and position of substituents in the stereoselectivity of the process is studied. The presence of a silyl group in the products provides an easy entry to further functionalization, dueto the ability of silicon to be oxidized under mild conditions (Fleming—Tamao oxidation). 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.

Références bibliographiques

  • Barbero, (2015), RSC Adv., 5, pp. 49541, 10.1039/C5RA06640A