Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose

Crystal structure of 1,2,3,4-di-O-methylene-α-d-galactopyranose

The title compound, C8H12O6, was synthesized by deacetylation of 6-acetyl-1,2,3,4-di-O-methylene-α-d-galactose with sodium methoxide. The central part of the molecule consists of a six-membered C5O pyranose ring with a twist-boat conformation. Both fused dioxolane rings adopt an envelope conformatio...

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Bibliographic Details
Main Authors: Ioannis Tiritiris, Stefan Tussetschläger, Willi Kantlehner
Format: Article
Language:English
Published: International Union of Crystallography 2015-12-01
Series:Acta Crystallographica Section E: Crystallographic Communications
Subjects:
crystal structure
deacetylation
D-galactose
O—H...O hydrogen bonds
C—H...O hydrogen bonds
Online Access:http://scripts.iucr.org/cgi-bin/paper?S2056989015021854

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http://scripts.iucr.org/cgi-bin/paper?S2056989015021854

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