Search Results - "MAULDIN, S. C"
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The Total Synthesis of Lipid I
Published in Journal of the American Chemical Society (25-07-2001)“…A total synthesis of lipid I (4), a membrane-associated intermediate in the bacterial cell wall (peptidoglycan) biosynthesis pathway, is reported. This highly…”
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Inhibition of human leukocyte elastase (HLE) by N-substituted peptidyl trifluoromethyl ketones
Published in Journal of medicinal chemistry (01-02-1992)“…A series of tripeptides possessing trifluoromethyl or aryl ketone residues at P1 were prepared and evaluated both in vitro and in vivo as potential inhibitors…”
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Synthesis and antiviral activity of prodrugs of the nucleoside 1-[2′,3′-Dideoxy-3′-C-(hydroxymethyl)-β- d-erythropentofuranosyl] cytosine
Published in Bioorganic & medicinal chemistry (01-05-1998)“…The synthesis and antiviral evaluation of 21 prodrugs of 1-[2′,3′-dideoxy-3′-C-(hydroxymethyl)-β- d-erythropentofuranosyl] cytosine 1 is reported. Cytosine N…”
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Synthesis of C-3 side-chain carboxylic acid cannabinoid derivatives
Published in Journal of heterocyclic chemistry (01-05-1985)“…Based upon the structural similarities of cannabinoid derivatives which inhibit the biosynthesis of prostaglandins with those of the potent inhibitor,…”
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Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 1. Tricyclic pyridobenzo- and dipyridodiazepinones
Published in Journal of medicinal chemistry (01-07-1991)“…Novel pyrido[2,3-b][1,4]benzodiazepinones (I), pyrido[2,3-b][1,5]benzodiazepinones (II), and dipyrido[3,2-b:2',3'-e][1,4]diazepinones (III) were found to…”
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The First Total Synthesis of Lipid II: The Final Monomeric Intermediate in Bacterial Cell Wall Biosynthesis
Published in Journal of the American Chemical Society (10-04-2002)“…Bacterial peptidoglycan is composed of a network of β-[1,4]-linked glyan strands that are cross-linked through pendant peptide chains. The final product, the…”
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Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. IV: 2-substituted dipyridodiazepinones as potent inhibitors of both wild-type and cysteine-181 HIV-1 reverse transcriptase enzymes
Published in Journal of medicinal chemistry (1995)Get full text
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