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METHYL-(2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL)-(1->3)-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-3-DEOXY-3-FLUORO-A

Compound with spectra: 1 NMR

METHYL-(2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL)-(1->3)-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-3-DEOXY-3-FLUORO-A
SpectraBase Compound ID 7JXwrkBE5aW
InChI InChI=1S/C27H46FNO18/c1-7-14(33)22(46-24-13(29-9(3)32)18(37)17(36)11(6-31)43-24)19(38)26(42-7)47-23-15(34)8(2)41-25(20(23)39)45-21-12(28)16(35)10(5-30)44-27(21)40-4/h7-8,10-27,30-31,33-39H,5-6H2,1-4H3,(H,29,32)
InChIKey JSVBVWOWOLFONW-UHFFFAOYSA-N
Mol Weight 691.7 g/mol
Molecular Formula C27H46FNO18
Exact Mass 691.269892 g/mol

View Spectrum of METHYL-(2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL)-(1->3)-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-3-DEOXY-3-FLUORO-A

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Propyl 3-O-(3-O-<2-acetamido-2-deoxy-B-D-glucopyranosyl>-2-O--A-L-rhap)-A-L-rhamnopyranoside
METHYL 2-O-[2-O-(2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-3-O-(ALPHA-D-GLUCOPYRANOSYL)-ALPHA-L-RHAMNOPYRANOSYL]-ALPHA-L-RHAMNOPYRANOSIDE
METHYL 3-O-(ALPHA-D-GLUCOPYRANOSYL)-2-O-[2-O-(2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-ALPHA-L-RHAMNOPYRANOSYL]-ALPHA-L-RHAMNOPYRANOSIDE
8-METHOXYCARBONYLOCTYL-2-O-(ALPHA-L-FUCOPYRANOSYL)-3-O-(2-N-ACETAMIDO-2-DEOXY-ALPHA-D-GALACTOPYRANOSYL)-BETA-D-GALACTOPYRANOSIDE;A-TRISACCHARIDE
ALPHA-D-GALNAC-(1->3)-BETA-D-GAL-(1->4)-[ALPHA-L-FUC-(1->3)]-BETA-D-GLCOME
METHYL-2-ACETAMIDO-2-DEOXY-3-O-[2-O-(ALPHA-L-FUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSYL]-BETA-D-GLUCOPYRANOSIDE
METHYL-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-O-ALPHA-D-GALACTOPYRANOSYL-(1->3)-2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
PROPYL-2-ACETAMIDO-2-DEOXY-3-O-[2-O-(ALPHA-L-FUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSYL]-BETA-D-GALACTOPYRANOSIDE
METHYL-O-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-O-2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSYL-(1->2)-ALPHA-L-RHAMNOPYRANOSIDE
Lacto-N-tetrose
Title Journal or Book Year
Synthesis of tri- and tetrasaccharide fragments of the Shigella dysenteriae type 1 O-antigen deoxygenated and fluorinated at position 3 of the methyl α-d-galactopyranoside terminus1Part 10 of the series Synthesis of ligands related to the O-specific antigen of Shigella dysenteriae type 1. For part 9 see ref[1].1 Carbohydrate Research 1998

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