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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-RHAMNOPYRANOSIDE

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-RHAMNOPYRANOSIDE
SpectraBase Compound ID mflhYNkPI3
InChI InChI=1S/C43H41ClO14/c1-25-33(55-39(47)28-18-10-5-11-19-28)35(36(42(50-3)51-25)56-40(48)29-20-12-6-13-21-29)58-43-37(57-41(49)30-22-14-7-15-23-30)34(53-31(45)24-44)32(26(2)52-43)54-38(46)27-16-8-4-9-17-27/h4-23,25-26,32-37,42-43H,24H2,1-3H3/t25-,26-,32-,33-,34+,35+,36+,37+,42+,43-/m1/s1
InChIKey QEPLQPISYIGDDJ-XVLXGJROSA-N
Mol Weight 817.2 g/mol
Molecular Formula C43H41ClO14
Exact Mass 816.218484 g/mol
Enantiomer InChIKey QEPLQPISYIGDDJ-ZYNLEWMVSA-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-RHAMNOPYRANOSIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
METHYL-O-(2,3,4-TRI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
METHYL 3-O-(2-O-ACETYL-3,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
METHYL 3-O-(3,4-DI-O-BENZOYL-BETA-L-RHAMNOPYRANOSYL)-2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
METHYL 3-O-(3,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
2,3,4-Tri-O-acetyl-.alpha.,L-rhamnopyranosyl-(1-3)-2,4-di-O-benzoyl-.alpha.,L-rhamnopyranose
METHYL 3-O-(2-O-ACETYL-4-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-4-O-BENZYL-2-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
Methyl 2,4-di-O-benzyl-3-O-(2,3,4-tri-O-acetyl.alpha.-L-rhamnopyranosyl).alpha.-L-rhamnopyranoside
METHYL 3-O-(4-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-4-O-BENZYL-2-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
ClEISTRIOSIDE-2;1-O-DODECANYL-3,4-DI-O-ACETYL-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-2,4-DI-O-ACETYL-ALPHA-L-RHAMNOPYRANOSYL-(1->3)-4-O-DIACETYL-ALPHA-L-RH
MEZZETTIAZIDE-11
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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