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hal.structure.identifierBioinorganic Laboratory, Department of Chemistry
dc.contributor.authorRAJSEKHAR, Gudneppanavar
hal.structure.identifierBioinorganic Laboratory, Department of Chemistry
dc.contributor.authorRAO, Chebrolu P.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorGUIONNEAU, Philippe
dc.date.issued2003
dc.identifier.issn0008-6215
dc.description.abstractEnβ-d-Ribopyranosylamine was synthesized and characterized using analytical, spectral and single-crystal X-ray diffraction methods. The molecule exists in the chair form with the 4C1 conformation. The β anomeric form of C-1 is supported by the dihedral angles. The molecule exhibits both intra- and intermolecular hydrogen-bond interactions of the type O---Hcdots, three dots, centeredO, N---Hcdots, three dots, centeredO and C---Hcdots, three dots, centeredO, and these are interconnected to each other to form chains.
dc.language.isoen
dc.publisherElsevier
dc.subject.enD-Ribopyranosylamine
dc.subject.enSingle-crystal X-ray diffraction
dc.subject.enGlycosyl amines
dc.title.enFirst crystallographic evidence for the formation of β-Image-ribopyranosylamine from the reaction of ammonia with of Image-ribose
dc.typeArticle de revue
dc.identifier.doi10.1016/S0008-6215(03)00006-5
dc.subject.halChimie/Matériaux
bordeaux.journalCarbohydrate Research
bordeaux.page801-805
bordeaux.volume338
bordeaux.issue8
bordeaux.peerReviewedoui
hal.identifierhal-00242736
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00242736v1
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