| ŠTANCL, Marek, Zuzana GARGULÁKOVÁ a Vladimír ŠINDELÁŘ. Glycoluril Dimer Isomerization under Aqueous Acidic Conditions. The Journal of Organic Chemistry. Columbus, OH, USA: the American Chemical Society, 2012, roč. 77, č. 23, s. 10945-10948. ISSN 0022-3263. Dostupné z: https://dx.doi.org/10.1021/jo302063j. |
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@article{1078093,
author = {Štancl, Marek and Garguláková, Zuzana and Šindelář, Vladimír},
article_location = {Columbus, OH, USA},
article_number = {23},
doi = {http://dx.doi.org/10.1021/jo302063j},
keywords = {cucurbiturils; glycolurils; isomerization; dimers},
language = {eng},
issn = {0022-3263},
journal = {The Journal of Organic Chemistry},
title = {Glycoluril Dimer Isomerization under Aqueous Acidic Conditions},
url = {http://pubs.acs.org/doi/abs/10.1021/jo302063j},
volume = {77},
year = {2012}
}
TY - JOUR
ID - 1078093
AU - Štancl, Marek - Garguláková, Zuzana - Šindelář, Vladimír
PY - 2012
TI - Glycoluril Dimer Isomerization under Aqueous Acidic Conditions
JF - The Journal of Organic Chemistry
VL - 77
IS - 23
SP - 10945-10948
EP - 10945-10948
PB - the American Chemical Society
SN - 00223263
KW - cucurbiturils
KW - glycolurils
KW - isomerization
KW - dimers
UR - http://pubs.acs.org/doi/abs/10.1021/jo302063j
L2 - http://pubs.acs.org/doi/abs/10.1021/jo302063j
N2 - A water-soluble methylene-bridged glycoluril dimer 2S was isolated. It was shown that 2S is the only kinetic product of the reaction between glycoluril derivative 1 and paraformaldehyde. Compound 2S is subsequently intermolecularly transformed into its diastereomer 2C. The kinetics and thermodynamics of the S- to C-shaped dimer isomerization were investigated under reaction conditions similar to those for cucurbituril synthesis.
ER -
ŠTANCL, Marek, Zuzana GARGULÁKOVÁ a Vladimír ŠINDELÁŘ. Glycoluril Dimer Isomerization under Aqueous Acidic Conditions. \textit{The Journal of Organic Chemistry}. Columbus, OH, USA: the American Chemical Society, 2012, roč.~77, č.~23, s.~10945-10948. ISSN~0022-3263. Dostupné z: https://dx.doi.org/10.1021/jo302063j.
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