Phenol–Quinone Tautomerism in (Arylazo)naphthols and the Analogous Schiff Bases: Benchmark Calculations-Reference-Cited by-同舟云学术

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Phenol–Quinone Tautomerism in (Arylazo)naphthols and the Analogous Schiff Bases: Benchmark Calculations

Published:2014-01-21 Issue:4 Volume:118 Page:778-789
ISSN:1089-5639
Container-title:The Journal of Physical Chemistry A
language:en
Short-container-title:J. Phys. Chem. A

Author:

Ali S. Tahir¹²,Antonov Liudmil³,Fabian Walter M. F.²

Affiliation:

1. Department of Chemistry, Federal Urdu University of Arts, Science & Technology, Karachi, Sindh, Pakistan

2. Institut für Chemie, Karl-Franzens-Universität Graz, Heinrichstrasse 28, A-8010 Graz, Austria

3. Institute of Organic Chemistry with Centre of Phytochemistry, Bulgarian Academy of Sciences, Sofia 1113, Bulgaria

Publisher

American Chemical Society (ACS)

Subject

Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp411502u

Reference104 articles.

1. The SAMPL2 blind prediction challenge: introduction and overview

2. Prediction of tautomer ratios by embedded-cluster integral equation theory

3. Some conclusions regarding the predictions of tautomeric equilibria in solution based on the SAMPL2 challenge

4. Blind prediction test of free energies of hydration with COSMO-RS

5. Prediction of SAMPL2 aqueous solvation free energies and tautomeric ratios using the SM8, SM8AD, and SMD solvation models

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3. Prototropic Tautomerism of 3-Nitro- and 5-Nitrosalicylidene-3-picolylimines;Russian Journal of General Chemistry;2022-05

4. Synthesis of Phenolic Coumestans via a Sequential Dehydrogenation/Oxa-Michael Addition Reaction of 2′,4′-Dihydroxyl-3-arylcoumarins;The Journal of Organic Chemistry;2022-04-14

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