Kinetic and Mechanistic Studies of the Deuterium Exchange in Classical Keto−Enol Tautomeric Equilibrium Reactions-Reference-Cited by-同舟云学术

Kinetic and Mechanistic Studies of the Deuterium Exchange in Classical Keto−Enol Tautomeric Equilibrium Reactions

Published:2010-07-08 Issue:9 Volume:87 Page:952-955
ISSN:0021-9584
Container-title:Journal of Chemical Education
language:en
Short-container-title:J. Chem. Educ.

Author:

Nichols Michael A.¹,Waner Mark J.¹

Affiliation:

1. Department of Chemistry, John Carroll University, University Heights, Ohio 44118

Publisher

American Chemical Society (ACS)

Subject

Education,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ed100292r

Reference8 articles.

1. Adapted fromGarland, C. W., Nibler, J. W., and Shoemaker, D. P.Experiments in Physical Chemistry,8th ed. (and earlier editions);McGraw-Hill:New York, 2008; pp466−474.

2. An NMR study of keto-enol tautomerism in β[beta]-dicarbonyl compounds

3. Hydrogen Bonding Using NMR: A New Look at the 2,4-Pentanedione Keto-Enol Tautomer Experiment

4. Determination of Solvent Effects on Keto—Enol Equilibria of 1,3-Dicarbonyl Compounds Using NMR

5. Jacobsen, N. E.NMR Spectroscopy Explained: Simplified Theory, Applications and Examples for Organic Chemistry and Structural Biology;Wiley-Interscience:New York, 2007; p131.

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