Solvent Effects on the Thioamide Rotational Barrier: An Experimental and Theoretical Study
Author:
Affiliation:
1. Contribution from the Department of Chemistry, Yale University, New Haven, Connecticut 06520-8107
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja003586y
Reference52 articles.
1. Amides. 3. Experimental and Theoretical Studies of the Effect of the Medium on the Rotational Barriers for N,N-Dimethylformamide and N,N-Dimethylacetamide
2. Gaussian‐2 theory using reduced Mo/ller–Plesset orders
3. Gas-phase carbon-13 NMR spectra and exchange kinetics of N,N-dimethylformamide
4. Why Does Thioformamide Have a Larger Rotational Barrier Than Formamide?
5. Gas-Phase NMR Studies of N,N-Dimethylthioamides. Influence of the Thiocarbonyl Substituent on the Internal Rotation Activation Energies
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