1H and C-13 NMR Study of the Molecular Structure of New Di-(β-Keto) Schiff bases
- 1 April 1990
- journal article
- research article
- Published by Taylor & Francis in Spectroscopy Letters
- Vol. 23 (4) , 447-457
- https://doi.org/10.1080/00387019008054427
Abstract
New di-(β-keto) schiff bases were prepared. The molecular structure of those di-(β-keto) schiff bases was determined by 1H and C-13 nmr spectroscopy.Keywords
This publication has 7 references indexed in Scilit:
- Carbon-13 nuclear magnetic resonance studies of aromatic compounds: comparison of hydrogen bonding effects in phenols, anilides, and anilinesJournal of the Chemical Society, Perkin Transactions 2, 1979
- Chemical constituents of gentianaceae. VIII The structure of gentiocrucine, a novel lactonic enamino ketoneTetrahedron Letters, 1974
- Carbon-13 Chemical Shifts and Intramolecular Hydrogen BondingThe Journal of Physical Chemistry, 1964
- Nuclear Magnetic Resonance Studies of Keto-Enol Equilibria. IV. Naphthalene DerivativesJournal of the American Chemical Society, 1963
- Nuclear Magnetic Resonance Studies of Keto-enol Equilibria. III. α,β-Unsaturated-β-KetoaminesJournal of the American Chemical Society, 1962
- A Proton Resonance Study of Bis-(acetylacetone)-ethylenediimine and Related Schiff BasesJournal of the American Chemical Society, 1961
- 185. Reactions of alkylisoformanilides. Part III. With phenolsJournal of the Chemical Society, 1947