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METHYL-(2,4-DI-O-BENZOYL-3-O-CHLOROACETYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-(2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-4,6-O-BENZYLIDE

Compound with spectra: 1 NMR

METHYL-(2,4-DI-O-BENZOYL-3-O-CHLOROACETYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-(2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-4,6-O-BENZYLIDE
SpectraBase Compound ID 49vAPD8EuAh
InChI InChI=1S/C56H54ClFO18/c1-31-41(70-49(60)33-19-9-4-10-20-33)45(69-39(59)29-57)47(72-51(62)35-23-13-6-14-24-35)56(67-31)76-46-42(71-50(61)34-21-11-5-12-22-34)32(2)66-55(48(46)73-52(63)36-25-15-7-16-26-36)75-44-40(58)43-38(68-54(44)64-3)30-65-53(74-43)37-27-17-8-18-28-37/h4-28,31-32,38,40-48,53-56H,29-30H2,1-3H3/t31-,32-,38-,40+,41-,42-,43+,44-,45+,46+,47+,48+,53?,54+,55-,56-/m0/s1
InChIKey HBGLJWVEENJGEV-SVKRLYTASA-N
Mol Weight 1069.5 g/mol
Molecular Formula C56H54ClFO18
Exact Mass 1068.298271 g/mol
Enantiomer InChIKey HBGLJWVEENJGEV-DZTWMZQOSA-N

View Spectrum of METHYL-(2,4-DI-O-BENZOYL-3-O-CHLOROACETYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-(2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-4,6-O-BENZYLIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
METHYL-(2,3,4-TRI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-(2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-4,6-O-BENZYLIDENE-3-DEOXY
METHYL-(2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-(2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-4,6-O-BENZYLIDENE-3-DEOXY-3-FLUO
ETHYL-[2,3-DI-O-BENZOYL-4,6-O-BENZYLIDENE-BETA-D-GLUCOPYRANOSYL-(1->4)]-2,3,6-TRI-O-BENZOYL-1-THIO-BETA-D-GLUCOPYRANOSIDE
#13A;2-(TRIMETHYLSILYL)-ETHYL-[2-O-ACETYL-4,6-O-BENZYLIDINE-3-O-[(TERT.-BUTOXYCARBONYL)-METHYL]-BETA-D-GALACTOPYRANOSYL]-(1->4)-[2,3,4-TRI-O-ACETYL-ALPHA-L-FUC
O-(2,4-DI-O-BENZOYL-ALPHA-D-RHAMNOPYRANOSYL)-(1->2)-O-(3,4-DI-O-BENZOYL-ALPHA-D-RHAMNOPYRANOSYL)-(1->3)-4-O-BENZOYL-1,2-O-(1-CYANOETHYLIDENE)-BETA-D-RHAMNOPYRANOSE
METHYL-2,3-DI-O-BENZOYL-5,6-O-ISOPROPYLIDENE-BETA-D-GALACTOFURANOSYL-(1->3)-2-O-ACETYL-4,6-O-BENZYLIDENE-ALPHA-D-MANNOPYRANOSIDE
#38;ALLYL-(3,4-DI-O-BENZYL-2-O-CHLOROACETYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-(3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-[2,3,4,6-TETRA-O-BENZYL-ALP
METHYL 2-O-BENZOYL-4-O-BENZYL-3-O-[4-O-BENZYL-3-O-(2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL)-2-O-(2,3,4-TETRA-O-ACETYL-ALPHA-L-RHAMNOPYRANOSYL)-ALPHA-L-RHAMNOPYRANOSYL]-ALPHA-L-RHAMNOPYRANOSIDE
#12;[4-O-BENZOYL-3-O-TERT.-BUTYLDIMETHYLSILYL-2,6-DIDEOXY-2-IODO-ALPHA-D-MANNO-HEXOPYRANOSYL]-(1->2)-METHYL-(3-O-BENZYL-4,6-O-BENZYLIDENE-BETA-D-GLUCOPYRANOSI
O-(3-O-ACETYL-2,4-DI-O-BENZOYL-ALPHA-D-RHAMNOPYRANOSYL)-(1->2)-O-(3,4-DI-O-BENZOYL-BETA-D-RHAMNOPYRANOSYL)-(1->3)-4-O-BENZOYL-1,2-O-(1-CYANOETHYLIDENE)-BETA-D-RHAMNOPYRANOSE
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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