4-(Dimethoxymethyl)phenyl 2,3,4,6-tetra-<i>O</i>-acetyl-β-<scp>D</scp>-glucopyranoside

Zipp, Caitlin F.; Fernandes, Manuel A.; Marques, Helder M.; Michael, Joseph P.

doi:10.1107/s160053681201121x

Acta Cryst E

2012

DOI: 10.1107/s160053681201121x

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4-(Dimethoxymethyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Caitlin F. Zipp

Manuel A. Fernandes

Helder M. Marques

et al.

Abstract: The enantiomerically pure title compound, C23H30O12, crystallizes in the chiral space group P212121. The O-acetylated-glucopyranoside moiety adopts a chair conformation. Numerous C—H⋯O interactions as well as a C—H⋯π interaction are present in the crystal structure.

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4-(Dimethoxymethyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Abstract: The enantiomerically pure title compound, C23H30O12, crystallizes in the chiral space group P212121. The O-acetylated-glucopyranoside moiety adopts a chair conformation. Numerous C—H⋯O interactions as well as a C—H⋯π interaction are present in the crystal structure.

Cited by 0 publications

References 10 publications

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4-(Dimethoxymethyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Abstract: The enanti­omerically pure title compound, C23H30O12, crystallizes in the chiral space group P212121. The O-acetyl­ated-glucopyran­oside moiety adopts a chair conformation. Numerous C—H⋯O inter­actions as well as a C—H⋯π inter­action are present in the crystal structure.

Cited by 0 publications

References 10 publications

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Abstract: The enantiomerically pure title compound, C23H30O12, crystallizes in the chiral space group P212121. The O-acetylated-glucopyranoside moiety adopts a chair conformation. Numerous C—H⋯O interactions as well as a C—H⋯π interaction are present in the crystal structure.