27064-40-0Relevant academic research and scientific papers
Quantitative Treatment of the Solvent Influence on the Rate of the Reaction of Amines with N-(Methylthiochloromethylene)arenesulfonamides
Makitra,Vasyutyn,Pirig
, p. 826 - 830 (2007/10/03)
The rate of the reaction of N-(methylthiochloromethylene)arenesulfonamide chlorides with amines is determined by the basicity of the medium, its increase facilitating elimination of hydrogen chloride from the intermediate charge transfer complex formed by
Strukturanalytische Untersuchungen an Folgeprodukten aus Sulfonamiden VI - Kinetische Untersuchungen zur Reaktion von N-Arylsulfonyl-iminothiokohlensaeuremethylesterchloriden mit aliphatischen Aminen
Hans, M.,Imrich, J.,Barnikol, F.,Reinke, H.,Suchar, G.,et al.
, p. 1089 - 1097 (2007/10/02)
The reaction of a number of N-arylsulfonyl-iminothiocarbonic acid methylesterchloride compounds 1 with nucleophiles is studied by means of stopped-flow analysis.To clarify the reaction mechanism the influence of concentration, solvents and substituents on
SYNTHESIS AND PROPERTIES OF N3-SUBSTITUTED N1,N2-BISARYLSULFONYLGUANIDINES
Dubina, V. L.,Dobronravov, A. N.
, p. 1731 - 1734 (2007/10/02)
N3-Substituted N1,N2-bisarylsulfonylguanidines were obtained by the amidation of derivatives of N-arylsulfonylcarbonimidic acid.Their structural similarity to butamide (N1-p-tolylsulfonyl-N2-butylurea) and cyclamide (N1-p-tolylsulfonyl-N2-cyclohexylurea) and also the similarity of some their chemical characteristics are not determining factors in the manifestation of sugar-decreasing characteristics by these guanidine derivatives.
