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METHYL-4-DEOXY-3-C-[(S)-1,2-DIHYDROXYETHYL]-2,3'':3,3'-DI-O-ISOPROPYLIDENE-ALPHA-D-XYLOPYRANOSIDE

Compound with spectra: 1 NMR

METHYL-4-DEOXY-3-C-[(S)-1,2-DIHYDROXYETHYL]-2,3'':3,3'-DI-O-ISOPROPYLIDENE-ALPHA-D-XYLOPYRANOSIDE
SpectraBase Compound ID C4099IgZ8Kj
InChI InChI=1S/C15H26O7/c1-13(2)18-8-10-15(22-14(3,4)20-10)6-9(7-16)19-12(17-5)11(15)21-13/h9-12,16H,6-8H2,1-5H3
InChIKey BXPMHOUQUFFMQV-UHFFFAOYSA-N
Mol Weight 318.37 g/mol
Molecular Formula C15H26O7
Exact Mass 318.167853 g/mol

View Spectrum of METHYL-4-DEOXY-3-C-[(S)-1,2-DIHYDROXYETHYL]-2,3'':3,3'-DI-O-ISOPROPYLIDENE-ALPHA-D-XYLOPYRANOSIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
METHYL-4-DEOXY-3-C-[(S)-1,2-DIHYDROXYETHYL]-3,3'-ISOPROPYLIDENE-3'',6-BIS-O-(3,5-DINITROBENZOYL)-ALPHA-D-XYLOHEXOPYRANOSIDE
(2'R)-1,2;5,6-Di-O-isopropylidene-3-C-(2-hydroxy-2-phenylethyl)-.alpha.,D-glucofuranose
3-C-[2-(Hydroxymethyl)phenylmethyl]-1,2:5,6-di-O-isopropylidenr-.alpha.,D-allofuranose
(2'S)-1,2;5,6-Di-O-isopropylidene-3-C-(2-hydroxy-2-phenylethyl)-.alpha.,D-glucofuranose
(3S)-Pentacarbonyl{3-[1',2':3',4'-di-O-isopropylidene-.alpha.,L-5'-arabinopyranosyl]-5-methylene-2-oxacyclopentylidene}chromium(0)
.alpha.-D-Glucopyranose, O-2,3,4,6-tetra-O-acetyl-.beta.-D-glucopyranosyl-(1.fwdarw.2)-O-[2,3, 4,6-tetra-O-acetyl-.beta.-D-glucopyranosyl-(1.fwdarw.6)]-, triacetate
3',4',6'-TRI-O-ACETYL-2'-DEOXY-2'-FLUORO-ALPHA-D-MANNOPYRANOSYL-(1'->4)-1,6-ANHYDRO-2,3-O-ISOPROPYLIDENE-BETA-D-MANNOPYRANOSE
NEWBOULDIOSIDE;2-(3,4-DIHYDROXYPHENYL)-ETHYL-O-BETA-D-APIOFURANOSYL-(1->2)-O-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-6-O-E-FERULOYL-BETA-D-GLUCOPYRANOSIDE
MARKHAMIOSIDE-B;3-HYDROXY-4-METHOXY-BETA-PHENYLETHOXY-O-[BETA-APIOFURANOSYL-(1''''->2'')-ALPHA-RHAMNOPYRANOSYL-(1'''->3'')-6''-O-FERULOYL-BETA-GLUCOPYRAN
(1S*,2R*,6S*,7R*)-1-Methoxy-4,4,7-trimethyl-3,5,9,12-tetraoxatricyclo[5.4.1.0(2,6)]dodecan-10-one
Title Journal or Book Year
Deoxygenation at C-4 and Stereospecific Branched-Chain Construction at C-3 of a Methyl Hexopyranuloside. Synthetic Approach to the Amipurimycin Sugar Moiety The Journal of Organic Chemistry 1996
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