The hydrolytic reactivity of B-sultams

Baxter, Nicholas J., Laws, Andrew P., Rigoreau, Laurent and Page, Michael I. (1996) The hydrolytic reactivity of B-sultams. Journal of the Chemical Society, Perkin Transactions 2 (11). p. 2245. ISSN 1472-779X

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Abstract

N-Methyl -sultam undergoes acid- and base-catalysed hydrolysis in water at 30 °C and I= 1.0 mol dm–3 with kH+= 2.79 dm3 mol–1s–1 and kOH= 1.38 × 10–2 dm3mol–1 s–1. These second-order rate constants are approximately 109 and 107, respectively, greater than those for a similar acyclic sulfonamide. The entropy of activation for the acid-catalysed hydrolysis of the -sultam is –80 J K–1 mol–1 which may be indicative of unimolecular ring opening, whereas that for the base-catalysed reaction, –184 J K–1 mol–1, is consistent with a bimolecular process.

Item Type:	Article
Subjects:	Q Science > Q Science (General) Q Science > QD Chemistry
Schools:	School of Applied Sciences
Related URLs:	Author Author
Depositing User:	Sharon Beastall
Date Deposited:	05 Nov 2009 12:32
Last Modified:	07 Apr 2018 14:15
URI:	http://eprints.hud.ac.uk/id/eprint/6096

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