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Competitive endo- and exo-cyclic C-N fission in the hydrolysis of N-aroyl β-lactams

Tsang, Wing Y., Ahmed, Naveed, Hemming, Karl and Page, Michael I. (2005) Competitive endo- and exo-cyclic C-N fission in the hydrolysis of N-aroyl β-lactams. Canadian Journal of Chemistry, 83 (9). pp. 1432-1439. ISSN 1480-3291

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Abstract

Abstract: The balance between endo- and exo-cyclic C–N fission in the hydrolysis of N-aroyl β-lactams shows that the difference in reactivity between strained β-lactams and their acyclic analogues is minimal. Attack of hydroxide ion occurs preferentially at the exocyclic acyl centre rather than that of the β-lactam during the hydrolysis of N-p-nitrobenzoyl β-lactam. In general, both endo- and exo-cyclic C–N bond fission occurs in the alkaline hydrolysis of N-aroyl β-lactams, the ratio of which varies with the aryl substituent. Hence, the Brønsted β-values differ for the two processes: –0.55 for the ring-opening reaction and –1.54 for the exocyclic C–N bond fission reaction. For the pH-independent and acid-catalysed hydrolysis of N-benzoyl β-lactam, less than 3% of products are derived from exocyclic C–N bond fission.

Item Type: Article
Subjects: Q Science > Q Science (General)
Q Science > QD Chemistry
Schools: School of Applied Sciences
School of Applied Sciences > Biomolecular Sciences Research Centre
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Depositing User: Sara Taylor
Date Deposited: 08 Feb 2008 10:26
Last Modified: 24 Aug 2010 13:57
URI: http://eprints.hud.ac.uk/id/eprint/512

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