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Azetidine-2,4-diones (4-oxo-beta-lactams) as scaffolds for designing elastase inhibitors

Jalmira Mulchande1, Rita C Guedes, Wing-Yin Tsang

  • 1iMed UL, CECF, Faculdade de Farmácia, Universidade de Lisboa, Av. Forças Armadas, Lisbon, Portugal.

Journal of Medicinal Chemistry
|February 23, 2008
PubMed

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The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para position.