Substituent Effects on the Patterns of Intermolecular Interactions of 3-Alkyl and 3-Cycloalkyl Derivatives of Phenytoin: A Crystallographic and Quantum-Chemical Study-Reference-Cited by-同舟云学术

Substituent Effects on the Patterns of Intermolecular Interactions of 3-Alkyl and 3-Cycloalkyl Derivatives of Phenytoin: A Crystallographic and Quantum-Chemical Study

Published:2019-03-08 Issue:4 Volume:19 Page:2163-2174
ISSN:1528-7483
Container-title:Crystal Growth & Design
language:en
Short-container-title:Crystal Growth & Design

Author:

Trišović Nemanja¹^ORCID,Radovanović Lidija²^ORCID,Janjić Goran V.³,Jelić Stefan T.⁴,Rogan Jelena¹

Affiliation:

1. Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade, Serbia

2. Innovation Center, Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade, Serbia

3. Institute of Chemistry, Technology and Metallurgy, University of Belgrade, Njegoševa 12, 11000 Belgrade, Serbia

4. Institute for Multidisciplinary Research, University of Belgrade, Kneza Višeslava 1, 11000 Belgrade, Serbia

Funder

Ministarstvo Prosvete, Nauke i Tehnolo?kog Razvoja

Publisher

American Chemical Society (ACS)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.cgd.8b01776

Reference41 articles.

1. Phenytoin: an old but effective antiarrhythmic agent for the suppression of ventricular tachycardia

2. Class 1B agents lidocaine, mexiletine, tocainide, phenytoin

3. Assessment of the effect of phenytoin on cutaneous healing from excision of melanocytic nevi on the face and on the back

4. Phenytoin as a novel anti-vitiligo weapon

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