SciELO - Scientific Electronic Library Online

 
vol.65Simultaneous multi-element electrothermal atomic absorption determination using a low resolution CCD spectrometer and continuum light source: The concept and methodologyA DFT and NBO analysis of the bonding in titanocenyl complexes containing a five-membered L,L'-cyclic ligand: L,L' = O,O'; S,S' or Se,Se' author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

    Related links

    • On index processCited by Google
    • On index processSimilars in Google

    Share


    South African Journal of Chemistry

    On-line version ISSN 1996-840XPrint version ISSN 0379-4350

    Abstract

    VAN ES, Theodorus; STASKUN, Benjamin  and  KARUSO, Peter. The transposing of isomer yields in the methanolyses of N-substituted quinolinimides by triethylamine. S.Afr.j.chem. (Online) [online]. 2012, vol.65, pp.53-61. ISSN 1996-840X.

    The effect of triethylamine in transposing the respective yields of the two isomeric esters ensuing from the methanolysis of N-substituted quinolinimides is described and is rationalized with a mechanism.

    Keywords : N-Substituted quinolinimides; methyl 2-carbamoyl-3-pyridinecarboxylates; methyl 3-carbamoyl-2-pyridinecarboxylates; benzenesulfonamide derivatives; triethylamine-induced rearrangements; reaction mechanisms.

            · text in English     · English ( pdf )