Synthesis of Flavin-Calix[4]arene Conjugate Derivatives
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F11%3A43892805" target="_blank" >RIV/60461373:22310/11:43892805 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1002/hlca.201000260" target="_blank" >http://dx.doi.org/10.1002/hlca.201000260</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/hlca.201000260" target="_blank" >10.1002/hlca.201000260</a>
Alternative languages
Result language
angličtina
Original language name
Synthesis of Flavin-Calix[4]arene Conjugate Derivatives
Original language description
The synthesis of two new flavin substituted calix[4]arene derivatives, 9 and 10, is described. The first flavin substituted calix[4]arene derivative 9 was synthesized by the reaction of 3-methylalloxazine (5)with 25,27-bis(3-bromopropoxy)-26,28-dihydroxy-5,11,17,23-tetra(tert-butyl)calix[4]arene (4) in high yield (92%). The other derivative 10 was prepared from methylalloxazine-1-acetic acid (7) and 25,27-bis(3-cyanopropoxy)calix[4]arene (3). All new compounds were characterized by a combination of FTIRand 1H-NMR spectroscopy, and elemental-analysis techniques.
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
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Helvetica Chimica Acta
ISSN
0018-019X
e-ISSN
—
Volume of the periodical
94
Issue of the periodical within the volume
3
Country of publishing house
CH - SWITZERLAND
Number of pages
5
Pages from-to
481-485
UT code for WoS article
000288464600019
EID of the result in the Scopus database
—