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Synthesis of p-nitro- and o-nitro-phenyl-β-D-xylopyranoside

✍ Scribed by F. G. Loontiens; C. K. Bruyne


Book ID
104855529
Publisher
Springer
Year
1964
Tongue
English
Weight
166 KB
Volume
51
Category
Article
ISSN
0028-1042

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In the title compound, C 20 H 23 NO 12 , the pyranoside ring adopts a 4 C 1 chair conformation, with all substituents oriented in equatorial positions. The endocyclic C-O-C angle is in agreement with the geometry of the equatorial glycosidic bond, typical for the -d-4 C 1 pyranoside conformation.