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- W2091697224 abstract "3′-Episeldomycin 5 (7) was synthesized from seldomycin 5. Reaction of hexa-N-ethoxycarbonylseldomycin 5 (2) with o-nitrobenzenesulfonyl chloride gave penta-N-ethoxycarbonylseldomycin 5-2′,3′-epicyclic carbamate (3) in one step. Hexa-N-ethoxycarbonyl-3′-O-tosylseldomycin 5 or hexa-N-ethoxycarbonyl-3′-O-mesylseldomycin 5, prepared from 2, was also converted into 3 by being heated in weakly basic solvents such as N,N-dimethylformamide or pyridine. Compound 3 was hydrolyzed to give 7. Structure of 7 was confirmed by PMR, CMR, MS, and Δ[M] values. Compound 7 was found to be active against resistant bacteria which carry 3′-O-phosphorylating enzymes. Δ[M] values for vicinal amino groups were shortly discussed." @default.
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- W2091697224 date "1977-11-01" @default.
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- W2091697224 title "Chemical Transformation of Seldomycin 5 into 3′-Episeldomycin 5 and Its Antibacterial Activity" @default.
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- W2091697224 doi "https://doi.org/10.1246/bcsj.50.3039" @default.
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