Abstract
A short, enantioselective, and diastereoselective synthesis of cytoxazone, a Th2-selective immunomodulator from Streptomyces, is described. The route was readily adapted to the synthesis of the three other stereoisomers of natural cytoxazone. Evaluation of these compounds revealed that the stereochemical configuration of the oxazolidinone ring did not influence their biological activity. © 2003 Elsevier Science Ltd. All rights reserved.
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CITATION STYLE
Carter, P. H., LaPorte, J. R., Scherle, P. A., & Decicco, C. P. (2003). A new synthesis of cytoxazone and its diastereomers provides key initial SAR information. Bioorganic and Medicinal Chemistry Letters, 13(7), 1237–1239. https://doi.org/10.1016/S0960-894X(03)00131-8
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