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Stereochemical investigations of the methyl α-D-threo- and ethyl α-D-erythro- anomers of 4,6-di-O-acetyl-2,3-dideoxyhex-2-enopyranoside by X-ray diffraction methods

✍ Scribed by Krajewski, J. W. ;Urbańczyk-Lipkowska, Z. ;Gluziński, P. ;Bleidelis, J. ;Kemme, A.


Book ID
114526453
Publisher
International Union of Crystallography
Year
1979
Weight
500 KB
Volume
35
Category
Article
ISSN
0567-7408

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4,6-Di-O-acetyl-2,3-dideoxy-D-erythro-hex-2-enopyranose (4,6-di-o-acetyl-D-pseudoglucal), prepared from 3,4,6-tri-O-acetyl-1,5-anhydro-2-deoxy-D-arubinohex-1-enitol (tri-0-acetyl-D-glucal), was condensed, by catalysis with boron trifluoride, with an equivalent of the original glycal, to give crystal