#39;ALLYL-(3,4-DI-O-BENZYL-2-O-PARA-METHOXYBENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-(3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-[2,3,4,6-TETRA-O-BENZ
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 5kpHF07WiaL |
|---|---|
| InChI | InChI=1S/C98H106O20/c1-6-56-102-95-93(115-94(99)79-50-32-15-33-51-79)89(84(69(4)111-95)116-97-91(109-64-77-48-30-14-31-49-77)88(108-63-76-46-28-13-29-47-76)85(105-60-73-40-22-10-23-41-73)81(114-97)66-101-57-70-34-16-7-17-35-70)117-98-92(87(107-62-75-44-26-12-27-45-75)83(68(3)113-98)104-59-72-38-20-9-21-39-72)118-96-90(110-65-78-52-54-80(100-5)55-53-78)86(106-61-74-42-24-11-25-43-74)82(67(2)112-96)103-58-71-36-18-8-19-37-71/h6-55,67-69,81-93,95-98H,1,56-66H2,2-5H3/t67-,68-,69+,81-,82-,83-,84+,85-,86+,87+,88+,89-,90+,91-,92+,93-,95-,96-,97-,98-/m1/s1 |
| InChIKey | XMKFAPBCNSLTGS-GELDCWKRSA-N |
| Mol Weight | 1603.9 g/mol |
| Molecular Formula | C98H106O20 |
| Exact Mass | 1602.727746 g/mol |
| Enantiomer InChIKey | XMKFAPBCNSLTGS-YPMLSEHKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
;#40;ALLYL-(3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-(3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-[2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANO
#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
#10;ALLYL-(3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-[2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL-(1->4)]-2-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSIDE
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
Bzl 3-O-bzl-2-O-(2,3,4,6-tetraac-B-D-glucopyranosyl)-4-O-(2,3,4,6-tetrabzl-A-D-galactopyranosyl)-A-L-rhamnopyranoside
#19;[6-[2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL-(1->4)-2,3-DI-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL-(1->4)-2,3,6-TRI-O-BENZYL-1-METHOXY-ALPHA-D-GLUCOPYRANOS-6-
2-BENZYLOXYCARBONYLAMINOETHYL 2-O-[2,4-DI-O-BENZYL-3-O-(3,6-DIDEOXY-2,4-DI-O-PARA-NITROBENZOYL-ALPHA-D-XYLOHEXOPYRANOSY;)-ALPHA-L-RHAMNOPYRANOSYL]-3,4,6-TRI-O-BENZYL-ALPHA-D-MANNOPYRANOSIDE
2-BENZYLOXYCARBONYLAMINOETHYL 2-O-[2,4-DI-O-BENZYL-3-O-(3,6-DIDEOXY-2,4-DI-O-PARA-NITROBENZOYL-ALPHA-D-XYLOHEXOPYRANOSYL)-BETA-L-RHAMNOPYRANOSYL]-3,4,6-TRI-O-BENZYL-ALPHA-D-MANNOPYRANOSIDE
METHYL 4,6-DI-O-BENZYL-2-O-(2,3,4,6-TETRA-O-BENZYL-BETA-D-GLUCOPYRANOSYL)-3-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSIDE
METHYL 4,6-DI-O-BENZYL-2-O-(2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL)-3-O-(2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYL)-BETA-D-GALACTOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Blockwise Approach to Fragments of the O-Specific Polysaccharide of Shigella flexneri Serotype 2a: Convergent Synthesis of a Decasaccharide Representative of a Dimer of the Branched Repeating Unit1 | The Journal of Organic Chemistry | 2004 |