The kinetics and mechanism of a highly efficient intramolecular nucleophilic reaction. The cyclization of ethyl N-[o-(N-hydroxycarbamoyl)benzoyl]-carbamate to N-hydroxyphthalimide
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1988/P2/P29880000213
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2. Unusual Effects of Pure Nonionic and Mixed Nonionic–Cationic Micelles on the Rate of Alkaline Hydrolysis ofN-Hydroxyphthalimide;Journal of Dispersion Science and Technology;2010-06-24
3. Kinetics and mechanism of tertiary amine-catalyzed cleavage ofN′-morpholino-N-(2′-methoxyphenyl)phthalamide: Kinetic evidence for the presence of a reactive intermediate on the reaction path;International Journal of Chemical Kinetics;2010-05
4. Experimental versus theoretical evidence for the rate-limiting steps in uncatalyzed and H+ - and HO− -catalyzed hydrolysis of the amide bond;International Journal of Chemical Kinetics;2009-06-22
5. Kinetics and mechanism of large rate enhancement in an acidic aqueous cleavage of the tertiary amide bond of N-(2-methoxyphenyl)-N′-morpholinophthalamide (1);Bioorganic Chemistry;2008-08
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