Heteroatom Chemistry · 2008 · 17 citations · 6 references
Natural SciencesChemistryMedicinal ChemistryBioorganic ChemistryGreen ChemistryOrganic ChemistryAmino Acid ChemistryAntifungal AgentsAmino Acid EstersAntimicrobial MetabolitesMass Spectral Data AnalysisNew Antifungal Agents
Abstract Synthesis of several 5,5‐dimethyl‐2‐oxido‐[1,3,2]‐dioxaphosphorinane‐2‐yl‐amino carboxylates ( 4a–j ) was accomplished through a two‐step process. This involves prior preparation of the intermediate monochloride ( 2 ), 2‐chloro‐5,5‐dimethyl [1,3,2]dioxaphosphorinane‐2‐oxide and its subsequent reaction with various amino acid esters ( 3a–j ) in dry tetrahydrofuran in the presence of triethyl amine at room temperature. They were characterized by elemental analysis, IR, 1 H, 13 C, 31 P NMR, and mass spectral data. Their antifungal and antibacterial activity is also evaluated. Majority of these compounds exhibited moderate antimicrobial activity in the assay. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:256–260, 2008; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/hc.20426
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Adam Siddiqui, Carlo Ballatore, Christopher McGuigan et al. · Journal of Medicinal Chemistry · 1999 · 76 citations
Carston R. Wagner, Edward J. McIntee, Raymond F. Schinazi et al. · Bioorganic & Medicinal Chemistry Letters · 1995 · 53 citations
Novel phosphate derivatives of zidovudine as anti-HIV compounds