Resolution of pentafluorophenyl 2-phenylpropanoate using combinations of quasi-enantiomeric oxazolidin-2-ones

Al Shaye, Najla; Benoit, David M.; Chavda, Sameer; Coulbeck, Elliot; Dingjan, Marco; Eames, Jason; Yohannes, Yonas

doi:10.1016/j.tetasy.2011.02.022

Authors

Najla Al Shaye

Dr David Benoit D.Benoit@hull.ac.uk
Senior Lecturer in Molecular Physics and Astrochemistry

Sameer Chavda

Elliot Coulbeck

Marco Dingjan

Jason Eames J.Eames@hull.ac.uk

Yonas Yohannes

Abstract

The kinetic, mutual and parallel resolution of a series of structurally related active esters derived from 2-phenylpropanoic acid using a combination of quasi-enantiomeric oxazolidin-2-ones is discussed.

Citation

Al Shaye, N., Benoit, D. M., Chavda, S., Coulbeck, E., Dingjan, M., Eames, J., & Yohannes, Y. (2011). Resolution of pentafluorophenyl 2-phenylpropanoate using combinations of quasi-enantiomeric oxazolidin-2-ones. Tetrahedron: Asymmetry, 22(4), 413-438. https://doi.org/10.1016/j.tetasy.2011.02.022

Journal Article Type	Article
Acceptance Date	Feb 24, 2011
Online Publication Date	Mar 30, 2011
Publication Date	Feb 24, 2011
Journal	TETRAHEDRON-ASYMMETRY
Print ISSN	0957-4166
Electronic ISSN	1362-511X
Publisher	Elsevier
Peer Reviewed	Peer Reviewed
Volume	22
Issue	4
Pages	413-438
DOI	https://doi.org/10.1016/j.tetasy.2011.02.022
Keywords	Physical and Theoretical Chemistry; Inorganic Chemistry; Organic Chemistry; Catalysis
Public URL	https://hull-repository.worktribe.com/output/399982
Publisher URL	https://www.sciencedirect.com/science/article/pii/S0957416611001078?via%3Dihub