Acetyl α-<scp>D</scp>-2,3,4-triacetyllyxopyranoside

The structure of the title compound, C<sub>13</sub>H<sub>18</sub>O<sub>9</sub>, has monoclinic (<i>P</i>2<sub>1</sub>) symmetry. It is of inter-est with respect to stereochemistry and the anomeric effect. Two acetyl subsituents adopt equatorial orientations and two are axial. The extended structure displays C-H⋯O hydrogen bonding.

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IUCrData
Published
2025-01-10
DOI
https://doi.org/10.1107/s2414314625000161
Primary Topic
Synthesis of Organic Compounds
Type
article
Field-Weighted Citation Impact
0.00

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article

Acetyl α-D-2,3,4-triacetyllyxopyranoside

Jonathan S. Rhoad, Shawn Culver
IUCrData
Synthesis of Organic Compounds
article

Acetyl α-D-2,3,4-triacetyllyxopyranoside

Jonathan S. Rhoad, Shawn Culver
article en

Abstract

The structure of the title compound, C<sub>13</sub>H<sub>18</sub>O<sub>9</sub>, has monoclinic (<i>P</i>2<sub>1</sub>) symmetry. It is of inter-est with respect to stereochemistry and the anomeric effect. Two acetyl subsituents adopt equatorial orientations and two are axial. The extended structure displays C-H⋯O hydrogen bonding.

IUCrDataVol. 10(1)
Missouri Western State University (US)
National Science Foundation, Division of Chemistry
Clean water and sanitation
Openalex Percentile: Top 99%
Synthesis of Organic Compounds
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Acetyl α-<scp>D</scp>-2,3,4-triacetyllyxopyranoside — Jonathan S. Rhoad, Shawn Culver · IUCrData (2025) | TGRS Research Map | TGRS