Indexed keywords
4 N (4 METHYLPHENYL)UREIDO 25,26,27,28 TETRAPROPOXYTHIACALIX[4]ARENE;
4 N (4 NITROPHENYL)UREIDO 25,26,27,28 TETRAPROPOXYTHIACALIX[4]ARENE;
4,16 BIS[N' (4 NITROPHENYL)UREIDO] 25,26,27,28 TETRAPROPOXYTHIACALIX[4]ARENE;
4,16 BIS[N' (4 TOLYL)UREIDO] 25,26,27,28 TETRAPROPOXYTHIACALIX[4]ARENE;
4,18 BIS[N' (4 NITROPHENYL)UREIDO] 25,26,27,28 TETRAPROPOXYTHIACALIX[4]ARENE;
4,18 BIS[N' (4 TOLYL)UREIDO] 25,26,27,28 TETRAPROPOXYTHIACALIX[4]ARENE;
ANION;
CALIXARENE;
DIMETHYL SULFOXIDE;
UNCLASSIFIED DRUG;
ARTICLE;
CHIRALITY;
COMPLEX FORMATION;
CONFORMATION;
NITRATION;
PRIORITY JOURNAL;
REDUCTION;
STEREOISOMERISM;
SUBSTITUTION REACTION;
SYNTHESIS;
1
50249151074
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Gutsche, C.D.1
13
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For review on calixarene-based anion receptors see: V.I. Kalchenko Pure Appl. Chem. 80 2008 1449 1458
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Kalchenko, V.I.1
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For some recent examples of urea-substituted calixarene-based receptors from our group see: P. Cuřínová, I. Stibor, J. Budka, J. Sykora, K. Lang, and P. Lhoták New J. Chem. 33 2009 612 619
(2009)
New J. Chem.
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Cuřínová, P.1
Stibor, I.2
Budka, J.3
Sykora, J.4
Lang, K.5
Lhoták, P.6
18
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I. Stibor, J. Budka, V. Michlová, M. Tkadlecová, M. Pojarová, P. Cuřínová, and P. Lhoták New J. Chem. 32 2008 1597 1607
(2008)
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Stibor, I.1
Budka, J.2
Michlová, V.3
Tkadlecová, M.4
Pojarová, M.5
Cuřínová, P.6
Lhoták, P.7
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J. Kroupa, I. Stibor, M. Pojarova, M. Tkadlecova, and P. Lhotak Tetrahedron 64 2008 10075 10079
(2008)
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Kroupa, J.1
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Lhotak, P.5
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K. Lang, P. Curinová, M. Dudic, P. Prosková, I. Stibor, V. Stastny, and P. Lhoták Tetrahedron Lett. 46 2005 4469 4472
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Lang, K.1
Curinová, P.2
Dudic, M.3
Prosková, P.4
Stibor, I.5
Stastny, V.6
Lhoták, P.7
22
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For some examples of anion receptors based on urea-substituted calixarene in the 1,3-alternate conformation see: B. Schazmann, N. Alhashimy, and D. Diamond J. Am. Chem. Soc. 128 2006 8607 8614
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Filby, M.H.1
Dickson, S.J.2
Zaccheroni, N.3
Prodi, L.4
Bonacchi, S.5
Montalti, M.6
Chiorboli, C.7
Paterson, M.J.8
Humphries, T.D.9
Steed, J.W.10
25
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For reviews on thiacalixarenes, see: N. Morohashi, F. Narumi, N. Iki, T. Hattori, and S. Miyano Chem. Rev. 106 2006 5291 5316
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Chem. Rev.
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Morohashi, N.1
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Iki, N.3
Hattori, T.4
Miyano, S.5
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O. Kundrat, J. Kroupa, S. Böhm, J. Budka, V. Eigner, and P. Lhotak J. Org. Chem. 75 2010 8372 8375
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Kundrat, O.1
Kroupa, J.2
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Lhotak, P.6
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O. Kundrat, I. Cisarova, B. Böhm, M. Pojarova, and P. Lhotak J. Org. Chem. 74 2009 4592 4596
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Kundrat, O.1
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Lhotak, P.5
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O. Kundrat, H. Dvorakova, I. Cisarova, M. Pojarova, and P. Lhotak Org. Lett. 11 2009 4188 4191
(2009)
Org. Lett.
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Kundrat, O.1
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Pojarova, M.4
Lhotak, P.5
32
80053054007
The biding constants were calculated using the computer program OPIUM (Kyvala M.) freely available at: http://www.natur.cuni.cz/∼kyvala/opium. html. All our attempts to measure the stoichiometry of complexes using Job plot analysis have failed as the small complexation constants did not lead to well resolved maximum in the corresponding plots. Anyhow, the complexation curves gave the best fit using 1:1 stoichiometry.
33
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