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TETRA-O-ACETYL-BETA-D-RIBOFURANOSE
SpectraBase Compound ID 7UsQYIJJFOR
InChI InChI=1S/C13H18O9/c1-6(14)18-5-10-11(19-7(2)15)12(20-8(3)16)13(22-10)21-9(4)17/h10-13H,5H2,1-4H3/t10-,11-,12-,13-/m0/s1
InChIKey IHNHAHWGVLXCCI-CYDGBPFRSA-N
Mol Weight 318.28 g/mol
Molecular Formula C13H18O9
Exact Mass 318.095082 g/mol
Enantiomer InChIKey IHNHAHWGVLXCCI-FDYHWXHSSA-N
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • PERACETYL-BETA-D-RIBOSE,(FURANOSE)
  • 1,2,3,5-TETRAACETYL-BETA-D-RIBOFURANOSE
  • 1,2,3,5-TETRA-O-ACETYL-BETA-L-RIBOFURANOSIDE
Title Journal or Book Year
Reaction Kinetics and Mechanism of Sulfuric Acid-Catalyzed Acetolysis of Acylated Methyl L-Ribofuranosides European Journal of Organic Chemistry 2009
Triazolopyridine nucleosides. II. Glycosylations of 3-oxo-s-triazolo[4,3-a]pyridines with accompanying conversions into 2-oxo-s-triazolo[1,5-a]pyridine nucleosides Canadian Journal of Chemistry 1977
Syntheses, structural and conformational assignments, and conversions of pyridine and triazolopyridine nucleosides Canadian Journal of Chemistry 1976

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