Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28610%2F17%3A63517212" target="_blank" >RIV/70883521:28610/17:63517212 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.3390/M925" target="_blank" >http://dx.doi.org/10.3390/M925</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/M925" target="_blank" >10.3390/M925</a>
Alternative languages
Result language
angličtina
Original language name
Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate
Original language description
Ethyl({[acryloyl(furan-2-ylmethyl)amino]acetyl}amino)acetate was synthesized via Ugi four component (4C) reaction at ambient temperature. The protocol employs a reaction between formaldehyde, furfurylamine, acrylic acid, and ethyl 2-isocyanoacetate. The course of the reaction was found to be high yielding, and the resulting glycine ester derivative was well characterized by elemental analysis, FTIR, NMR spectroscopy, and mass spectrometric techniques.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
MolBank
ISSN
1422-8599
e-ISSN
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Volume of the periodical
2017
Issue of the periodical within the volume
1
Country of publishing house
CH - SWITZERLAND
Number of pages
4
Pages from-to
1-4
UT code for WoS article
000418113500004
EID of the result in the Scopus database
2-s2.0-85009730038