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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

Authors

Najla Al Shaye

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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.

Journal Article Type Article
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
APA6 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
DOI https://doi.org/10.1016/j.tetasy.2011.02.022
Keywords Physical and Theoretical Chemistry; Inorganic Chemistry; Organic Chemistry; Catalysis
Publisher URL https://www.sciencedirect.com/science/article/pii/S0957416611001078?via%3Dihub


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