Access to enantioenriched 2,3- and 2,5-dihydrofurans with a fully substituted C2 stereocenter by Pd-catalyzed asymmetric intermolecular Heck reaction.
Journal article

Access to enantioenriched 2,3- and 2,5-dihydrofurans with a fully substituted C2 stereocenter by Pd-catalyzed asymmetric intermolecular Heck reaction.

  • Borrajo-Calleja GM Department of Organic Chemistry , University of Geneva , 30 quai Ernest Ansermet , 1211 Geneva-4 , Switzerland . Email: clement.mazet@unige.ch.
  • Bizet V Department of Organic Chemistry , University of Geneva , 30 quai Ernest Ansermet , 1211 Geneva-4 , Switzerland . Email: clement.mazet@unige.ch.
  • Bürgi T Department of Physical Chemistry , University of Geneva , 30 quai Ernest Ansermet , 1211 Geneva-4 , Switzerland.
  • Mazet C Department of Organic Chemistry , University of Geneva , 30 quai Ernest Ansermet , 1211 Geneva-4 , Switzerland . Email: clement.mazet@unige.ch.
  • 2017-11-17
Published in:
  • Chemical science. - 2015
English A palladium-catalyzed intermolecular asymmetric Heck reaction with dihydrofurans with a trisubstituted double bond is reported. The use of two different chiral ligands provides access to valuable 2,3- and 2,5-dihydrofurans with a fully substituted C2 stereocenter with high levels of regio- and enantiocontrol.
Language
  • English
Open access status
gold
Identifiers
Persistent URL
https://sonar.ch/global/documents/34338
Statistics

Document views: 17 File downloads: