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dc.creatorYan, Zhiqing
dc.creatorChang, Yuning
dc.creatorMayo, Dennis
dc.creatorMaslak, Veselin
dc.creatorXia, Shijing
dc.creatorBađić, Jovica D.
dc.date.accessioned2018-11-22T00:09:57Z
dc.date.available2018-11-22T00:09:57Z
dc.date.issued2006
dc.identifier.issn1523-7060
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/795
dc.description.abstractInspired by allostery in nature, we synthesized cavitand 1 and investigated regulation of its conformational dynamics. Quantitative H-1 NMR studies have revealed that the rate of the conformational isomerization of 1 can be modulated using the external addition of acid. As 1 maintains its vase-like conformation in an acidic environment, ample opportunities for controlling the kinetics of molecular recognition, and thus reactivity, in this and related receptors have arisen.en
dc.publisherAmer Chemical Soc, Washington
dc.rightsrestrictedAccess
dc.sourceOrganic Letters
dc.titleAllosteric regulation of the conformational dynamics of a cavitand receptoren
dc.typearticle
dc.rights.licenseARR
dcterms.abstractБадјиц, Јовица Д.; Цханг, Yунинг; Yан, Зхиqинг; Маyо, Деннис; Маслак, Веселин; Xиа, Схијинг;
dc.citation.volume8
dc.citation.issue17
dc.citation.spage3697
dc.citation.epage3700
dc.identifier.wos000239655500020
dc.identifier.doi10.1021/ol0612760
dc.citation.other8(17): 3697-3700
dc.citation.rankM21a
dc.identifier.pmid16898795
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-33748584333
dc.identifier.rcubKon_1748


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