Sulfur atom

introduced at different positions in ring C

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Synthesis and antibacterial activity of some thio trinems.
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Formation of cyclic sulfinates and sulfinamides through homolytic substitution at the sulfur atom
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Thioepoxide formation by ring closure of allylthiyl radicals - A novel rearrangement of allylic thionitrites
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The Stereochemical Outcome of the DAST Fluorination of 4'-Thiopyrimidine Nucleosides with "Up" Hydroxyl Groups is Controlled by the Oxidation State of the Sulfur Atom
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Convergent Synthesis of Some 2',3'-Dideoxy-3'-mercapto Nucleosides - Potential Anti-HIV Agents
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Synthesis of 6-thiatetracycline, a highly active analogue of the antibiotic tetracycline
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- 3-(2-Chloro-5-methoxy-phenylsulfanyl)-pentanedioic acid dimethyl ester

Synthesis Fluorination Palladium-catalyzed cross-coupling Rearrangement Chemical reactions Nucleophilic substitution Reagent Cyclic Antibacterial activity Minimum inhibitory concentration (MIC) Structure-activity relationships (SAR) Tert-butyldimethylsilyl (TBS) Lithium diisopropylamide (LDA) Ring closure Novel Substitution Conditions Convergent Synthesis Formation Experimental terms Text format Experiment Heterocyclic compound Antibiotic DAST Sulfinamides Homolytic substitution Oxidation state Analogue Reactive Intermediates Carbon-carbon double bond experimental synthesis Anti-HIV Agents Stereochemical outcome Nucleoside analogs

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