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dc.contributor.authorHaridas, V-
dc.contributor.authorSandhya, S-
dc.contributor.authorGeeta, H-
dc.contributor.authorSuresh, C H-
dc.date.accessioned2013-06-17T08:06:47Z-
dc.date.available2013-06-17T08:06:47Z-
dc.date.issued2012-10-10-
dc.identifier.citationTetrahedron Letters 53(41):5523-5527;10 Oct 2012en_US
dc.identifier.urihttp://hdl.handle.net/123456789/467-
dc.description.abstractAmino acid-based molecules containing a bis-urea moiety have been synthesized and demonstrated for their anion binding affinities. Compound 1c binds phosphate and sulfate with binding constants of 3.6 103 M 1 and 4.3 103 M 1, respectively. These molecules undergo proton transfer upon treatment with fluoride, resulting in the formation of imidazolidinediones. The crystal structure of one such diimidazolidinedione displays self-assembly through nonconventional hydrogen bonding interactionsen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectReceptorsen_US
dc.subjectUreaen_US
dc.subjectAnionsen_US
dc.subjectCyclizationen_US
dc.subjectImidazolidinedioneen_US
dc.title1,3-Phenyl linked urea-based receptors for anions and the facile cyclization to imidazolidinedioneen_US
dc.typeArticleen_US
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