Search Results - "Boujlel, K."

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  1. 1

    Voltammetric assay of Guaifenesin in pharmaceutical formulation by Tapsoba, I., Belgaied, J.-E., Boujlel, K.

    “…The electrochemical oxidation of Guaifenesin in a pharmaceutical formulation containing Guaifenesin has been carried out in Britton–Robinson buffer (BRB) (0.04…”
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  2. 2

    Electrochemical reduction of N-thioamidoimidates: application to the synthesis of thiazolo[5,4-d]thiazoles by Tapsoba, I., Medini, H., BenKhoud, M.L., Boujlel, K.

    “…The reduction of N-thioamidoimidates ( 1) has been examined in aprotic media at a mercury electrode. As shown by cyclic voltammetry at fast scan rates and…”
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  3. 3

    Electroxidation of ortho-substituted aromatic amines mechanistic investigation by Korbi, B.Haouas, Tapsoba, I., Benkhoud, M.L., Boujlel, K.

    “…The anodic oxidation of ortho-substituted aromatic amines has been investigated at a platinum electrode in aprotic solvent by cyclic voltammetry and controlled…”
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  4. 4

    Electrochemical synthesis of [1,2,4]oxadiazol-3-one derivatives: anodic oxidation of N-amidoimidates by Tapsoba, I., Adhoum, N., Khoud, M.L.Ben, Boujlel, K.

    “…Anodic oxidation of N-amidoimidates was performed in acetonitrile+lithium perchlorate as the electrolyte solution at platinum using controlled potentials. The…”
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  5. 5

    ELECTROCHEMICAL BEHAVIOUR OF HYDRAZONATES IN PROTIC AND APROTIC MEDIUM by Saied, T., Benkhoud, M. L., Boujlel, K.

    Published in Synthetic communications (01-01-2002)
    “…Cathodic reduction of several hydrazonates of a typical structure (Scheme 1 ) has been investigated by cyclic voltammetry and controlled potential electrolysis…”
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  6. 6

    REDUCTION OF N -2-SUBSTITUTED BENZIMIDAZOYL IMIDATES by Abderrahim, R., Medini, H., Kossai, R., Boujlel, K.

    Published in Synthetic communications (01-01-2002)
    “…Cathodic reduction of several iminoesters ( 1 ) and ( 2 ) has been investigated by cyclic voltammetry and controlled potential electrolysis at mercury…”
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  7. 7

    A New Route of Synthesis of 3a,6a-Dihydro-oxazolo[5,4-d]oxazole Derivatives by Tapsoba, I., Adhoum, N., Ben Khoud, M. L., Kossai, R., Boujlel, K.

    Published in Synthetic communications (06-01-2003)
    “…The electrochemical reduction of N-acylated imidates of a typical structure ( Sch. 1 ) has been investigated by cyclic voltammetry and controlled potential…”
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  8. 8
  9. 9

    Lead and cadmium concentrations in seawater and algae of the Tunisian coast by El Ati-Hellal, M, Hedhili, A, Hellal, F, Boujlel, K, Dachraoui, M, Bousnina, M, Ghorbel, H, Ndhif, M

    “…Both lead and cadmium are toxic trace metals, even in very weak concentrations. The aim of this study was to estimate lead and cadmium pollution in various…”
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  10. 10

    Determination of naproxen in pharmaceuticals by differential pulse voltammetry at a platinum electrode by Adhoum, Nafaâ, Monser, Lotfi, Toumi, Meriem, Boujlel, Khaled

    Published in Analytica chimica acta (24-10-2003)
    “…The anodic oxidation of naproxen has been carried out on a platinum electrode using cyclic, linear sweep and differential pulse voltammetry (DPV). Naproxen…”
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  11. 11

    Oxidation by heterogeneous and homogeneous electron transfer of N-amidoimidates: mechanistic investigation by Tapsoba, Issa, Haouas, Beya, Boujlel, Khaled

    “…Anodic oxidation of N-amidoimidates 1 was investigated in acetonitrile at a platinum electrode by means of cyclic voltammetry at low and high scan rates. The…”
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  12. 12

    Electrochemical Carboxylation of 2-Iodoaromatic Compounds by Haouas Korbi, B., Adhoum, N., Boujlel, K.

    Published in Synthetic communications (01-01-2004)
    “…The electrochemical reduction of a series of 2-iodoaromatic substituted compounds in acetonitrile under an atmospheric pressure of carbon dioxide leads to…”
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  13. 13
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    SYNTHESIS AND REACTVITY OF N-[N-PHOSPHORAMIDO-1H-BENZIMIDAZOL-2-YL] IMIDATES by Raouafi, Noureddine, Boujlel, Khaled, Benkhoud, Mohamed Lamine

    “…N-(-1H-Benzimidazol-2-yl) imidates 1a-c react with chlorophosphoramide to give the N-[-1-N,N,N′,N′-tetramethylphosphoramidoyl-1H-benzimidazol-2-yl]-imidates…”
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