Solvent Effects on the Barrier to Rotation in Carbamates
Author:
Affiliation:
1. Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9800863
Reference18 articles.
1. Nuclear magnetic resonance studies of amides
2. Theoretical study on structures and internal rotations of methylN,N-dimethylcarbamate and its sulphur, selenium, and tellurium homologues (Me2NC(O)YMe, Y = O,S,Se, Te)
3. Utilization of wieland furoxan synthesis for preparation of 4-aryl-1,2,5-oxadiazole-3-yl carbamate derivatives having potent anti-HIV activity
4. Catalysis of carbamate hydrolysis by vancomycin and semisynthetic derivatives
5. Barrier to internal rotation in amides. IV. N,N-Dimethylamides. Substituent and solvent effects
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