The title compound was isolated by several recrystallisations from a 1:l mixture of diastereomers which was obtained in 75% yield from the reaction of 1,2:3,4-di-O-isopropylidene-c~-D-galactopyranose with epichlorohydrin. The absolute configuration of this isomer (30% yield) was established by X-ray
β¦ LIBER β¦
Synthesis and Conformational Analysis of(6R)-[6-2H1]-1,2:3,4-Di-O-isopropylidene-.alpha.-D-galactopyranose. NMR and Molecular Modeling Studies
β Scribed by Midland, M. Mark; Asirwatham, Gitanjali; Cheng, John C.; Miller, Jennifer A.; Morell, Luis A.
- Book ID
- 126431218
- Publisher
- American Chemical Society
- Year
- 1994
- Tongue
- English
- Weight
- 534 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0022-3263
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