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Study of the structure of 4-amino-3-acetyl-6-methyl-2-pyrones by NMR

✍ Scribed by V. S. Bogdanov; V. V. Negrebetskii; F. A. Lakhvich; A. M. Moiseenkov; A. A. Akhrem


Book ID
112422115
Publisher
Springer
Year
1972
Tongue
English
Weight
311 KB
Volume
21
Category
Article
ISSN
1573-9171

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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,