The Hydrolysis of 4-Amino- and 4-Dimethylaminobenzene Sulfonyl Chlorides: An Unprecedented Case of Independence of Reactivity from pH
Author:
Affiliation:
1. Department of Chemistry and Industrial Chemistry, University of Genova, Via Dodecaneso, 31-16146 Genova, Italy, and CNR - Institute of Chemical Methodologies, Roma, Italy
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol1029113
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3. Perrin, D. D.; Dempsey, B.; Serjeant, E. P.pK Prediction of Organic acids and Bases;Chapman & Hall:London, 1982; p133.
4. The Properties of Electrolytes in Mixtures of Water and Organic Solvents. II. Ionization Constant of Water in 20, 45 and 70% Dioxane-Water Mixtures
5. A survey of Hammett substituent constants and resonance and field parameters
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1. Propanolysis of arenesulfonyl chlorides: Nucleophilic substitution at sulfonyl sulfur;Journal of Physical Organic Chemistry;2017-08-31
2. Isotope Effects in the Solvolysis of Sterically Hindered Arenesulfonyl Chlorides;International Journal of Chemical Kinetics;2015-09-22
3. Reactions of Carboxylic, Phosphoric, and Sulfonic Acids and their Derivatives;Organic Reaction Mechanisms Series;2014-04-04
4. The Hydrolysis of 4-Amino- and 4-Dimethylaminobenzene Sulfonyl Chlorides: An Unprecedented Case of Independence of Reactivity from pH;Organic Letters;2011-04-12
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