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Publikācija: Synthesis of 6-Sulfamoylsaccharin and Study of Its Reactivity in Alkylation Reactions

Publication Type Scientific article indexed in SCOPUS or WOS database
Funding for basic activity Unknown
Defending: ,
Publication language English (en)
Title in original language Synthesis of 6-Sulfamoylsaccharin and Study of Its Reactivity in Alkylation Reactions
Field of research 1. Natural sciences
Sub-field of research 1.4 Chemical sciences
Authors Jekaterīna Ivanova
Raivis Žalubovskis
Eriks Simins
Igor Vozny
Peteris Trapencieris
Keywords 6-sulfamoylsaccharin | alkylation | benzylation | oxidative cyclization | regioselectivity
Abstract An improved method for the preparation of 6-sulfamoylsaccharin (3-oxo-2,3-dihydro-1,2-benzo-thiazole-6-sulfonamide 1,1-dioxide) has been developed and studies of its possible direct alkylation have been carried out. It was shown that alkylation occurs regioselectively at the isothiazoline ring nitrogen atom. © 2012 Springer Science+Business Media, Inc.
DOI: 10.1007/s10593-012-0948-8
Hyperlink: http://link.springer.com/article/10.1007%2Fs10593-012-0948-8 
Reference Ivanova, J., Žalubovskis, R., Simins, E., Vozny, I., Trapencieris, P. Synthesis of 6-Sulfamoylsaccharin and Study of Its Reactivity in Alkylation Reactions. Chemistry of Heterocyclic Compounds, 2012, Vol.47, Iss.12, pp.1561-1564. ISSN 0009-3122. Available from: doi:10.1007/s10593-012-0948-8
Additional information Citation count:
ID 24031