Comparison of Reactivity of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium bromide with its N-Methyl and N,N-dimethyl derivative
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F03%3A00000749" target="_blank" >RIV/00216275:25310/03:00000749 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Comparison of Reactivity of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium bromide with its N-Methyl and N,N-dimethyl derivative
Original language description
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.
Czech name
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Czech description
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Classification
Type
D - Article in proceedings
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GP203%2F02%2FD170" target="_blank" >GP203/02/D170: Intramolecular Nucleophilic Substitution. Kinetics and Mechanism of the Tandem Recyclization Reaction</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2003
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Article name in the collection
10th Blue Danube Symposium on Heterocyclic Chemistry
ISBN
80-227-1938-2
ISSN
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e-ISSN
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Number of pages
1
Pages from-to
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Publisher name
Vydavatelstvo STU
Place of publication
Bratislava
Event location
Wien
Event date
Sep 3, 2003
Type of event by nationality
WRD - Celosvětová akce
UT code for WoS article
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