Reactivity study of tridecafluoro-5-trifluoromethyl-3,5-dioxanon-1-ene in nucleophilic reactions
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F02%3A00006544" target="_blank" >RIV/60461373:22310/02:00006544 - isvavai.cz</a>
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Reactivity study of tridecafluoro-5-trifluoromethyl-3,5-dioxanon-1-ene in nucleophilic reactions
Original language description
A series of nucleophiles were reacted with the title compound, all reactions were completely regioselective with the nucleophilic attack at the terminal carbon atom. Reactions of hydroxy compounds, thiols and cec-amines afforded addition products, whilebutyllithium, tributylphosphane or complex hydrides caused displacement of vinylic fluorine. Diethylamine and piperidine adducts displayed the property to substitute hydroxyl for fluorine.
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%2F1311" target="_blank" >GA203/01/1311: New generation of compounds for blood substitutes and other medicinal applications</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2002
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal Pharm.Science
ISSN
0022-3549
e-ISSN
—
Volume of the periodical
117
Issue of the periodical within the volume
2
Country of publishing house
BE - BELGIUM
Number of pages
11
Pages from-to
149-159
UT code for WoS article
—
EID of the result in the Scopus database
—