Comparative study of nucleophilic efficacy of pralidoxime towards phosphorus, sulphur and thiophosphorus based esters
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3AG44__%2F09%3A00002171" target="_blank" >RIV/60162694:G44__/09:00002171 - 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
Comparative study of nucleophilic efficacy of pralidoxime towards phosphorus, sulphur and thiophosphorus based esters
Original language description
Nucleophilic substitution reaction of p-nitrophenyldiphenyl phosphate, p-nitrophenyl p- toluene sulfonate and insecticide fenitrothion with pralidoxime have been studied at 27oC in the presence of different cationic surfactants. Micellar rate enhancements increase as the cationic head group is made less polar. The order of cleavage of different electrophilic centre by pralidoxime is P=O > S=O > P=S.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FP - Other medical fields
OECD FORD branch
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Result continuities
Project
<a href="/en/project/OVUOFVZ200803" target="_blank" >OVUOFVZ200803: Development of novel decontaminants and disinfectants of skin based on micellar compounds</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2009
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Reaction Kinetics and Catalysis Letters
ISSN
0133-1736
e-ISSN
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Volume of the periodical
98
Issue of the periodical within the volume
1
Country of publishing house
HU - HUNGARY
Number of pages
7
Pages from-to
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UT code for WoS article
000270190100012
EID of the result in the Scopus database
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