Kinetics and Mechanism of Ring Transformation of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium Bromide to 2-Methylimino-5-[2-(4-methoxyphenylamino)ethyl]thiazolidin-4-one
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F03%3A00000590" target="_blank" >RIV/00216275:25310/03:00000590 - isvavai.cz</a>
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Kinetics and Mechanism of Ring Transformation of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium Bromide to 2-Methylimino-5-[2-(4-methoxyphenylamino)ethyl]thiazolidin-4-one
Original language description
The kinetics and mechanism of ring transformation reaction of S-[1-(4-methoxyphenyl)pyrrolidin-2-on-3-yl]isothiuronium bromide was studied in aqueous amine buffers; general-base-catalyse changed into a specific one.
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—
Result continuities
Project
<a href="/en/project/GA203%2F01%2F0227" target="_blank" >GA203/01/0227: Intramolecular nucleophilic substitution. Extraordinary steric acceleration in a reaction of carbanion with electrophilic centre</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
Name of the periodical
Organic & Biomolecular Chemistry
ISSN
1477-0520
e-ISSN
—
Volume of the periodical
1
Issue of the periodical within the volume
7
Country of publishing house
GB - UNITED KINGDOM
Number of pages
6
Pages from-to
1204-1209
UT code for WoS article
—
EID of the result in the Scopus database
—