THE (C-5')-EPIMERIZATION OF AMINOGLYCOSIDES OF THE NEOMYCIN SERIES AIMING AT A STUDY �OF RESISTANT STRAINS INACTIVATING MECHANISMS AS WELL AS THE PREPARATION AND STUDY OF BIOLOGICALLY INTERESTING PYRAN DERIVATIVES
Abstract
THE SYNTHESIS OF THE (C-5') -EPIMERS OF NATURAL AMINOGLYCOSIDE ANTIBIOTICS OF IMPORTANT CLINICAL USE LIKE NEOMYCIN, PAROMOMYCIN AND RIBOSTAMYCIN IS THE MAIN ISSUE OF THE THESIS. THE SYNTHESIS OF THESE EPIMERIC PRODUCTS WILL ENABLE US TO DETERMINE THE BIOLOGICAL ROLE OF L-IDOPYRANOSYL-STRUCTURES IN AMINOGLYCOSIDE MOLECULES OF THE NEOMYCIN SERIES AND MAY LEAD TO NEW SYNTHETIC ANTIBIOTICS WITH ENHANCED ACTIVITY AGAINST RESISTANT STRAINS OF BACTERIA. THE DESIRED FINAL PRODUCTS MAY RESULT FOR 5'-EPI- PAROMAMINE AND 5'-EPI-NEAMINE THROUGH THE BIOCONVERSION OF THE LATTER BY MUTANTS D- (MUTATIONAL BIOSYNTHESIS). MODEL-WORKS WITH MONOSACCHARIDE ANALOGS FOR THE PREPARATION OF THESE SYNTHONS FROM NATURAL ANTIBIOTICS ARE DESCRIBED IN DETAIL AS WELL AS THE SYNTHESIS OF 5' -EPI-PAROMAMINE FROMPAROMOMYCIN. OTHER SYNTHETIC ISSUES DESCRIBED IN DETAIL ARE THE OXIDATIVE ACTION OF LEWIS ACIDS ON PARTIALLY BENZYLATED SUGARS WHICH WAS FOUND TO LEAD TO THESTEREOSPECIFIC SYNTHESIS OF 1,2-TRANS-FUSED DIOXANO- ...
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