Publikace detail

Comparison of Reactivity of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium bromide with its N-Methyl and N,N-dimethyl derivative

Autoři: Hanusek Jiří | Hejtmánková Ludmila | Sedlák Miloš

Rok: 2003

Druh publikace: článek ve sborníku

Název zdroje: 10th Blue Danube Symposium on Heterocyclic Chemistry

Název nakladatele: Vydavateľstvo Slovenskej technickej univerzity

Místo vydání: Bratislava

Strana od-do: PO-71

Tituly:

Jazyk	Název	Abstrakt	Klíčová slova
cze	Srovnání reaktivity S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiouronium bromidu s jeho N-methyl and N,N-dimethyl derivátem		mechanismus, kinetika, S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium salts, uzavírání cyklu
eng	Comparison of Reactivity of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium bromide with its N-Methyl and N,N-dimethyl derivative	Kinetics and mechanism of ring-transformation reaction of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3- yl]isothiuronium bromide and its N-methyl and N,N-dimethylderivative was studied in aqueous amine buffers. Changes in reaction pathway as well as type of catalysis have been observed.	mechanism, kinetics, S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium salts, ring closure,

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