Synthesis and biological investigation of new 4″-malonyl tethered derivatives of erythromycin and clarithromycin
摘要:
A new approach to 4 ''-substituted derivatives of erythromycin and clarithromycin was developed by converting them into corresponding 4"-malonic monoesters. Subsequent carbodiimide coupling with alcohols and amines provided new macrolide derivatives that are capable of binding to 50S ribosomal subunits and inhibiting protein synthesis in cell-free system. (C) 2005 Elsevier Ltd. All rights reserved.
Synthesis and biological investigation of new 4″-malonyl tethered derivatives of erythromycin and clarithromycin
摘要:
A new approach to 4 ''-substituted derivatives of erythromycin and clarithromycin was developed by converting them into corresponding 4"-malonic monoesters. Subsequent carbodiimide coupling with alcohols and amines provided new macrolide derivatives that are capable of binding to 50S ribosomal subunits and inhibiting protein synthesis in cell-free system. (C) 2005 Elsevier Ltd. All rights reserved.