Abstract
The design, synthesis and calcimimetic properties of various cyclic sulfonamides and sulfamates are described. The latter were prepared from the corresponding o-alkenylarenesulfonamides via copper- or rhodium-catalyzed intramolecular aziridination. The size of the cyclic sulfonamide rings as well as the position of the crucial (R)-naphthylethylamine substituent significantly affected calcimimetic activity. The most active compounds were the six- and seven-membered sulfonamides 30a and 31a and sulfamate 34a. © 2010 Elsevier Ltd. All rights reserved.
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Kiefer, L., Gorojankina, T., Dauban, P., Faure, H., Ruat, M., & Dodd, R. H. (2010). Design and synthesis of cyclic sulfonamides and sulfamates as new calcium sensing receptor agonists. Bioorganic and Medicinal Chemistry Letters, 20(24), 7483–7487. https://doi.org/10.1016/j.bmcl.2010.10.006
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