Crystal structure of 5-O-benzoyl-2,3-O-isopropylidene- D-ribono-1,4-lactone

dc.contributor.author	Bortoluzzi, Adailton João	pt_BR
dc.contributor.author	Silveira, Gustavo Pozza	pt_BR
dc.contributor.author	Sá, Marcus Mandolesi	pt_BR
dc.date.accessioned	2017-06-14T02:33:51Z	pt_BR
dc.date.issued	2017	pt_BR
dc.identifier.issn	2056-9890	pt_BR
dc.identifier.uri	http://hdl.handle.net/10183/159546	pt_BR
dc.description.abstract	In the title compound, C15H16O6, obtained from the acylation reaction between 2,3-O-isopropylidene-d-ribono-1,4-lactone and benzoyl chloride, the known absolute configuration for the lactone moiety of the ester substituent has been confirmed. The five-membered rings of the bicyclic lactone–dioxolane moiety both show envelope conformations and form a dihedral angle of 19.82 (7) between the lactone ring and the benzene ring. In the crystal, molecules of the acylated sugar are linked by very weak intermolecular C—H O interactions, forming a three-dimensional network.	en
dc.format.mimetype	application/pdf
dc.language.iso	eng	pt_BR
dc.relation.ispartof	Acta crystallographica section E: crystallographic communications. Chester. Vol. E73, no. 3 (Mar. 2017), p. 407-409	pt_BR
dc.rights	Open Access	en
dc.subject	Acilação	pt_BR
dc.subject	Estrutura cristalina	pt_BR
dc.subject	Interação intermolecular	pt_BR
dc.subject	Dinâmica molecular	pt_BR
dc.title	Crystal structure of 5-O-benzoyl-2,3-O-isopropylidene- D-ribono-1,4-lactone	pt_BR
dc.type	Artigo de periódico	pt_BR
dc.identifier.nrb	001015011	pt_BR
dc.type.origin	Estrangeiro	pt_BR

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