Five derivatives of methyl 3,4,6-triacetyl-2-deoxy-(3@-dialkylureido)-b-D-glucopyranoside were studied by 1H and 13C, NMR spectroscopy in solutions and by 13C NMR spectroscopy in the solid state. Sterically CDCl 3 crowded substituents such as n-hexyl and cylcohexyl change the chemical shifts of H-1,
β¦ LIBER β¦
A mechanistic study of the reaction of phenyl isocyanate with methyl 2,3,4-tri-O-acetyl-a-d-glucopyranoside
β Scribed by Spencer Knapp; Ronald P. Schreck; Yvon P. Carignan
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 381 KB
- Volume
- 203
- Category
- Article
- ISSN
- 0008-6215
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