Crook, S., Parr, N.J., Simmons, J. et al. (1 more author) (2014) Examining the origin of selectivity in the reaction of racemic alcohols with chiral N-phosphoryl oxazolidinones. Tetrahedron: Asymmetry, 25 (18-19). pp. 1298-1308. ISSN 0957-4166
Abstract
A range of known and novel N-phosphoryl oxazolidinones and imidazolidinones were prepared and screened in the kinetic resolution of a range of racemic magnesium chloroalkoxides. Models are proposed to account for the enantioselectivity achieved based on a combination of chiral relay effects, generation of transient stereochemistry and the structure of the intermediate magnesium alkoxide.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2014 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
Dates: |
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Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Science (Sheffield) > Department of Chemistry (Sheffield) |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 22 Mar 2016 14:09 |
Last Modified: | 22 Mar 2016 14:09 |
Published Version: | http://dx.doi.org/10.1016/j.tetasy.2014.08.003 |
Status: | Published |
Publisher: | Elsevier |
Refereed: | Yes |
Identification Number: | 10.1016/j.tetasy.2014.08.003 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:96468 |