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1,5-DIDEOXY-1,5-IMINO-D-(5D)-MANNITOL;1-DEOXY-(5D)-MANNONOJIRIMYCIN

Compound with spectra: 1 NMR

1,5-DIDEOXY-1,5-IMINO-D-(5D)-MANNITOL;1-DEOXY-(5D)-MANNONOJIRIMYCIN
SpectraBase Compound ID L7qWq89urOM
InChI InChI=1S/C6H13NO4/c8-2-3-5(10)6(11)4(9)1-7-3/h3-11H,1-2H2/t3-,4-,5-,6-/m1/s1/i3D
InChIKey LXBIFEVIBLOUGU-JNHZOBAGSA-N
Mol Weight 164.18 g/mol
Molecular Formula C6H122HNO4
Exact Mass 164.090735 g/mol
Enantiomer InChIKey LXBIFEVIBLOUGU-GLBDTLMASA-N

View Spectrum of 1,5-DIDEOXY-1,5-IMINO-D-(5D)-MANNITOL;1-DEOXY-(5D)-MANNONOJIRIMYCIN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
1-DEOXYMANNOJIRIMYCIN
1-DEOXYALLONOJIRIMYCIN
1,5-DIDEOXY-1,5-AMINO-D-GLUCITOL;(1-DEOXY-NOJIRIMICINE)
1,5-Dideoxy-1,5-imino-D-mannitol
DNJ;1-DEOXYNOJIRIMYCIN;1,6-13C-LABELED
1-DEOXY-GALACTOSTATIN;5-AMINO-1,5-DIDEOXY-D-GALACTOPYRANOSIDE
1-DEOXYALTRONOJIRIMYCIN
1-DEOXYNOJIRIMYCIN
1-DEOXY-MANNOJIRIMYCIN-HYDROCHLORIDE
(+)-1-DEOXYALLONOJIRIMYCIN-HYDROCHLORIDE
(2R,3R,4S,5R)-2-(HYDROXYMETHYL)-PIPERIDINE-3,4,5-TRIOL-HYDROCHLORIDE
1-DEOXYMANNOJIRIMYCIN
2,5-DIDEOXY-2,5-IMINO-D-(5D)-GLUCITOL
2,5-DIDEOXY-2,5-IMINO-D-(2D)-MANNITOL
1-DEOXYNOJIRIMYCIN-6-PHOSPHATE
(2R,3R,4R,5S)-2-[(1S)-1-hydroxyallyl]piperidine-3,4,5-triol
(2R,3R,4R,5S,6R)-2-(HYDROXYMETHYL)-6-PROPYL-PIPERIDINE-3,4,5-TRIOL
CUMDAMSIVYEHNL-QNVDADLQSA-N
2-ALPHA,3-BETA,6-EXO-TRIHYDROXY-NORTROPANE
N-(1R,2R,3S,4R)-HEX-5-YONIC-ACID-(2,3,4,5-TETRAHYDROXY-1-VINYL-PENTYL)-AMIDE
(4S,5R,6R,7S)-5,6-DIHYDROXY-4,7-DIHYDROXYMETHYL-1,3-DIAZEPAN-2-(N-BUTYL)-IMINIUM-TRIFLUOROACETATE
GALACTOSE_1,3-THIAZOLIDINE;MAJOR_DIASTEREOMER_C
Title Journal or Book Year
Synthesis of regio- and stereospecifically C-deuterated derivatives of glycosidase inhibitors 1-deoxymannonojirimycin and 2,5-dideoxy-2,5-imino-d-mannitol by intramolecular reductive amination employing deuterium gas1Dedicated to Professor Herfried Griengl on the occasion of his 60th birthday.1 Carbohydrate Research 1998

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