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J Antibiot (Tokyo) ; 42(6): 903-12, 1989 Jun.
Article in English | MEDLINE | ID: mdl-2500413

ABSTRACT

19-Deformyl-4'-deoxydesmycosin was synthesized by the following synthetic route: 19-Deformylation of desmycosin, 3,2',4''-tri-O-trimethylsilylation, 4'-O-sulfonylation, 4'-iodination, reductive deiodination and 3,2',4''-tri-O-detrimethylsilylation. Deformylation of the aldehyde group at the C-19 position was achieved by two different methods: A) A simple one-step deformylation using Wilkinson's catalyst ((Ph3P)3RhCl). B) Reductive decarboxylation of the 19-carboxyl derivative following NaClO2 oxidation of the aldehyde. 19-Deformyl-4'-deoxydesmycosin showed very strong antimicrobial activity in vitro and in vivo.


Subject(s)
Bacteria/drug effects , Leucomycins/chemical synthesis , Tylosin/analogs & derivatives , Animals , Biological Availability , Chemical Phenomena , Chemistry , Dogs , Enterococcus faecalis/drug effects , Leucomycins/pharmacokinetics , Leucomycins/pharmacology , Leucomycins/toxicity , Magnetic Resonance Spectroscopy , Male , Mass Spectrometry , Mice , Molecular Structure , Staphylococcal Infections/drug therapy , Staphylococcus aureus/drug effects , Streptococcal Infections/drug therapy , Streptococcus agalactiae/drug effects
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