Toward the Computational Design of Diastereomeric Resolving Agents: An Experimental and Computational Study of 1-Phenylethylammonium-2-phenylacetate Derivatives-Reference-Cited by-同舟云学术

Toward the Computational Design of Diastereomeric Resolving Agents: An Experimental and Computational Study of 1-Phenylethylammonium-2-phenylacetate Derivatives

Published:2007-04-19 Issue:19 Volume:111 Page:5326-5336
ISSN:1520-6106
Container-title:The Journal of Physical Chemistry B
language:en
Short-container-title:J. Phys. Chem. B

Author:

Karamertzanis Panagiotis G.¹,Anandamanoharan Parathy R.¹,Fernandes Phillipe¹,Cains Peter W.¹,Vickers Martin¹,Tocher Derek A.¹,Florence Alastair J.¹,Price Sarah L.¹

Affiliation:

1. Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, U.K., Department of Chemical Engineering, University College London, Torrington Place, London, WC1E 7JE, U.K., Avantium Technologies BV, Zekeringstraat 29, 1014 BV Amsterdam, The Netherlands, and Institute of Pharmacy & Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, Lanark, G4 0NR, U.K.

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp068530q

Reference63 articles.

1. Chiral separations

2. FDA's policy statement for the development of new stereoisomeric drugs.http://www.fda.gov/cder/guidance/stereo.htm. 6-7-0005.

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