Scientific article
OA Policy
English

New biphenyl iminium salt catalysts for highly enantioselective asymmetric epoxidation: role of additional substitution and dihedral angle

Published inOrganic & biomolecular chemistry, vol. 14, no. 18, p. 4220-4232
Publication date2016
Abstract

New biaryl iminium salt catalysts for enantioselective alkene epoxidation containing additional substitution in the heterocyclic ring are reported. The effects upon conformation and enantioselectivity of this additional substitution, and the influence of dihedral angle in these systems, has been investigated using a synthetic approach supported by density functional theory. Enantioselectivities of up to 97% ee were observed.

Research groups
Citation (ISO format)
BULMAN PAGE, Philip C. et al. New biphenyl iminium salt catalysts for highly enantioselective asymmetric epoxidation: role of additional substitution and dihedral angle. In: Organic & biomolecular chemistry, 2016, vol. 14, n° 18, p. 4220–4232. doi: 10.1039/C6OB00542J
Main files (1)
Article (Published version)
accessLevelPublic
Identifiers
Journal ISSN1477-0520
592views
231downloads

Technical informations

Creation05/04/2016 4:56:00 PM
First validation05/04/2016 4:56:00 PM
Update time03/15/2023 12:19:33 AM
Status update03/15/2023 12:19:32 AM
Last indexation10/31/2024 3:20:20 AM
All rights reserved by Archive ouverte UNIGE and the University of GenevaunigeBlack