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METHYL-3,4,5-TRI-O-ACETYL2,6-ANHYDRO-L-MANNO-HEXONATE

Compound with spectra: 1 NMR

METHYL-3,4,5-TRI-O-ACETYL2,6-ANHYDRO-L-MANNO-HEXONATE
SpectraBase Compound ID 2euy4H5dDIA
InChI InChI=1S/C13H18O9/c1-6(14)20-9-5-19-12(13(17)18-4)11(22-8(3)16)10(9)21-7(2)15/h9-12H,5H2,1-4H3/t9-,10-,11+,12+/m1/s1
InChIKey QJTZNWRABBGSCY-WYUUTHIRSA-N
Mol Weight 318.28 g/mol
Molecular Formula C13H18O9
Exact Mass 318.095082 g/mol
Enantiomer InChIKey QJTZNWRABBGSCY-NNYUYHANSA-N

View Spectrum of METHYL-3,4,5-TRI-O-ACETYL2,6-ANHYDRO-L-MANNO-HEXONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
METHYL-3,4,5-TRI-O-ACETYL-2,6-ANHYDRO-D-GALACTO-HEXONATE
METHYL-3,4,5-TRI-O-ACETYL-2,6-ANHYDRO-D-ALLO-HEXONATE
METHYL-3,4,5-TRI-O-ACETYL-2,6-ANHYDRO-D-GULO-HEXONATE
METHYL-3,4,5-TRI-O-ACETYL-2,6-ANHYDRO-D-ALTRO-HEXONATE
Gluconic acid ME5AC @
reduced and acetylated GalA
D-glucono-1,4-lactone tetraacetate
2,3,4-TRI-O-ACETYL-ALPHA-D-XYLOPYRANOSYL-TRICHLOROACETIMIDATE
O-(2,3,4-Tri-O-acetyl-a-d-arabinopyranosyl)-trichloroacetimidate
alpha-D-RIBOPYRANOSIDE, 2,3,4-TRI-O-ACETYL-beta-D-RIBOPYRANOSYL, TRIACETATE
Title Journal or Book Year
Syntheses of 2,6-anhydroaldonic acids from the corresponding anhydrodeoxynitroalditols (glycopyranosylnitromethanes) and their conversion into methyl esters, amides, and alditols Carbohydrate Research 1998

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