Crystal structure of 5-O-benzoyl-2,3-O-isopropylidene-d-ribono-1,4-lactone
Autor: | Adailton J. Bortoluzzi, Gustavo P. Silveira, Marcus M. Sá |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: | |
Zdroj: | Acta Crystallographica Section E: Crystallographic Communications, Vol 73, Iss 3, Pp 407-409 (2017) |
Druh dokumentu: | article |
ISSN: | 2056-9890 20569890 |
DOI: | 10.1107/S2056989017002043 |
Popis: | 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. |
Databáze: | Directory of Open Access Journals |
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