Analysis of Tautomerism in 􀀁-Ketobuanamides by Nuclear Magnetic Resonance: Substituent, Temperature and Solvent Effects

Journal of Applied Solution Chemistry and Modeling
doi 10.6000/1929-5030.2012.01.01.2
Full Text
Abstract

Available in full text

Date
Authors

Unknown

Publisher

Lifescience Global

Related search

KETO–ENOL TAUTOMERISM IN Β-Dicarbonyls STUDIED BY NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY: II. SOLVENT EFFECTS ON PROTON CHEMICAL SHIFTS AND ON EQUILIBRIUM CONSTANTS

Canadian Journal of Chemistry
Organic ChemistryCatalysisChemistry
1965English

The Nuclear Magnetic Resonance Spectra of Olefinic Protons and the Substituent Effects. V. Spin-Spin Coupling Intrans1,2-Disubstituted Ethylenes

Bulletin of the Chemical Society of Japan
Chemistry
1967English

Temperature-Controlled Molecular Depolarization Gates in Nuclear Magnetic Resonance

Angewandte Chemie - International Edition
CatalysisChemistry
2008English

Magnetic Ordering of TbMn2D2- A Nuclear Magnetic Resonance Analysis

Journal of Physics Condensed Matter
Materials ScienceCondensed Matter Physics
2001English

Variable Pressure and Temperature Nuclear Magnetic Resonance Study of Solvent Exchange on Manganese(II) Ion inN,N-Dimethylformamide. Influence of Solvent Molecular Size on Solvent Exchange Mechanism

Chemistry Letters
Chemistry
1987English

Theory of Nuclear Magnetic Resonance Detected by Nuclear Radiations

Physical Review A
1971English

Nuclear Magnetic Resonance

Nuclear Magnetic Resonance
BiochemistryAnalytical ChemistrySpectroscopy
2010English

Nuclear Magnetic Resonance

Nuclear Magnetic Resonance
BiochemistryAnalytical ChemistrySpectroscopy
2013English

Nuclear Magnetic Resonance

Nuclear Magnetic Resonance
BiochemistryAnalytical ChemistrySpectroscopy
1974English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy