Structure−Reactivity Relationships in the Pyridinolysis of N-Methyl-N-arylcarbamoyl Chlorides in Dimethyl Sulfoxide
Author:
Affiliation:
1. Department of Chemistry, Inha University, Inchon, 402-751 Korea, Department of Chemistry, Woosuk University, Chonju, 565-701 Korea, and Department of Science Education, Chonju National University of Education, Chonju, 560-757 Korea
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0108212
Reference41 articles.
1. Correlation of the Nucleophilic Reactivity of Aliphatic Amines
2. Kinetics of the hydrolysis of acyl chlorides in pure water
3. Kinetics of the hydrolysis of thiochloroformate esters in pure water
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1. Kinetics and Mechanism of the Pyridinolysis of O,O-Dimethyl S-Aryl Phosphorothioates in Dimethyl Sulfoxide;Bulletin of the Korean Chemical Society;2011-07-20
2. Nucleophilic Substitution Reactions of N-Methyl α-Bromoacetanilides with Benzylamines in Dimethyl Sulfoxide;Bulletin of the Korean Chemical Society;2011-03-20
3. Kinetics and mechanism of the pyridinolysis of N -aryl-P ,P -diphenyl phosphinic amides in dimethyl sulfoxide;Journal of Physical Organic Chemistry;2010-10-05
4. Michael-type Reactions of 1-(X-substituted phenyl)-2-propyn-1-ones with Alicyclic Secondary Amines in MeCN and H2O: Effect of Medium on Reactivity and Transition-State Structure;Bulletin of the Korean Chemical Society;2010-05-20
5. Regioselectivity and the Nature of the Reaction Mechanism in Nucleophilic Substitution Reactions of 2,4-Dinitrophenyl X-Substituted Benzenesulfonates with Primary Amines;The Journal of Organic Chemistry;2003-05-21
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