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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