In search of new erythromycin derivatives 3-O-[γ-(4-oxo-2-aryl- thiazolidin-3-yl)butyryl]erythromycin A derivatives have been synthesized. The 3-hydroxy group was derivatised to a primary amine and subsequently the thiazolidinone nucleus was generated at the amino functionality through DCC mediated one-pot three-component reaction in good yields. © 2008 Pandey et al; licensee Beilstein-Institut.
CITATION STYLE
Haq, W., Pandey, D., & Katti, S. B. (2008). New acylides: Synthesis of 3-O-[γ-(4-oxo-2-arylthiazolidin-3-yl) butyryl]erythromycin A derivatives. Beilstein Journal of Organic Chemistry, 4. https://doi.org/10.3762/bjoc.4.14
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