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pubmed-article:2737957pubmed:abstractTextThe synthesis and biological evaluation of D-forphenicinol-cephalosporins are described. 7-Amino-3-(substituted)-3-cephem-4-carboxylic acid esters were coupled with N-tert-butoxy-carbonyl-D-forphenicinol derivatives. Most of cephalosporin analogs in this series had good antibacterial activities and were well absorbed from the gastrointestinal tract in mice. Among them, 7-(mono-O-methyl-D-forphenicinol)-3-propenyl analog showed the most significant result in biological evaluations.lld:pubmed
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pubmed-article:2737957pubmed:articleTitleOrally absorbable D-forphenicinol-cephalosporins.lld:pubmed
pubmed-article:2737957pubmed:affiliationInstitute of Microbial Chemistry, Tokyo, Japan.lld:pubmed
pubmed-article:2737957pubmed:publicationTypeJournal Articlelld:pubmed