A quantum mechanical study of the mechanism of the enol‐ketone tautomerism
- 1 January 1979
- journal article
- Published by Wiley in Bulletin des Sociétés Chimiques Belges
- Vol. 88 (11) , 875-882
- https://doi.org/10.1002/bscb.19790881107
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Nitrosoacetaldehyde and its enol and oxime isomers. A theoretical investigation of an asymmetric 1,5-sigmatropic hydrogen shiftJournal of the American Chemical Society, 1979
- Keto-enol tautomerism. Relative stabilization of enol isomersAustralian Journal of Chemistry, 1978
- A theoretical treatment on the behavior of the hydrogen-bonded proton in malonaldehydeJournal of the American Chemical Society, 1977
- Correlation effects on barriers to proton transfer in intramolecular hydrogen bonds. The enol tautomer of malondialdehyde studied by ab initio SCF-CI calculationsJournal of the American Chemical Society, 1976
- Molecular orbital studies of hydrogen bonds. VIII. Malonaldehyde and symmetric hydrogen bonding in neutral speciesJournal of the American Chemical Society, 1975
- ab initio Molecular orbital study of the effects of α-substitution on keto–enol tautomerismJournal of the Chemical Society, Chemical Communications, 1972
- Ground states of σ-bonded molecules. Part XII. MINDO/1 studies of inversion barriers, rotational barriers, tautomerism, and hydrogen bondingJ. Chem. Soc. A, 1971
- Catalysis of α-Hydrogen Exchange. I. The Reaction of Isobutyraldehyde-2-d with Tertiary Amines and Oxygen Bases1aJournal of the American Chemical Society, 1965
- Nitrosation, diazotisation, and deaminationQuarterly Reviews, Chemical Society, 1961
- The Action of Nitrous Acid on Aliphatic AminesNature, 1960