Propargyl Anthranilate Derivatives and Their Application in the Synthesis of Rings Containing 1,2,3-Triazolo Motifs

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18470%2F13%3A50001337" target="_blank" >RIV/62690094:18470/13:50001337 - isvavai.cz</a>
Alternative codes found
RIV/61989592:15310/13:33147719
Result on the web
<a href="http://dx.doi.org/10.1002/jhet.1514" target="_blank" >http://dx.doi.org/10.1002/jhet.1514</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/jhet.1514" target="_blank" >10.1002/jhet.1514</a>

Result language
angličtina
Original language name
Propargyl Anthranilate Derivatives and Their Application in the Synthesis of Rings Containing 1,2,3-Triazolo Motifs
Original language description
Propargyl anthranilate, a simple and less studied molecule with several reactive sites, is widely applicable in organic synthesis. An optimized synthesis of this compound and its derivatives and the preparation of azide derivatives are described. The optimized process of the known intramolecular cyclization is described, and the unknown intermolecular cyclizations of these azido derivatives and formation of a macrocycle are discussed.
Czech name
—
Czech description
—

Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—

Project
<a href="/en/project/ME09057" target="_blank" >ME09057: Research of new organic compounds with anticancer activity with use of combinatorial chemistry</a><br>
Continuities
N - Vyzkumna aktivita podporovana z neverejnych zdroju

Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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