METHYL-ALPHA-D-[2,3,4-TRI-O-ACETYL-6-O-(4',6'-DI-O-ACETYL-2',3'-DIDEOXY-ALPHA-D-HEX-2'-ENOPYRANOSYL)]-GLUCOPYRANOSIDE
Compound with spectra: 1 NMR
![METHYL-ALPHA-D-[2,3,4-TRI-O-ACETYL-6-O-(4',6'-DI-O-ACETYL-2',3'-DIDEOXY-ALPHA-D-HEX-2'-ENOPYRANOSYL)]-GLUCOPYRANOSIDE](/api/compound/Iw5XTZjZ68t.png?ph=true&h=300&w=458 "METHYL-ALPHA-D-[2,3,4-TRI-O-ACETYL-6-O-(4',6'-DI-O-ACETYL-2',3'-DIDEOXY-ALPHA-D-HEX-2'-ENOPYRANOSYL)]-GLUCOPYRANOSIDE")
| SpectraBase Compound ID | Iw5XTZjZ68t |
|---|---|
| InChI | InChI=1S/C23H32O14/c1-11(24)30-9-17-16(32-12(2)25)7-8-19(36-17)31-10-18-20(33-13(3)26)21(34-14(4)27)22(35-15(5)28)23(29-6)37-18/h7-8,16-23H,9-10H2,1-6H3/t16-,17+,18+,19-,20+,21-,22+,23-/m1/s1 |
| InChIKey | XUESHPUQOWYBRW-JCMWOGNFSA-N |
| Mol Weight | 532.5 g/mol |
| Molecular Formula | C23H32O14 |
| Exact Mass | 532.179206 g/mol |
| Enantiomer InChIKey | XUESHPUQOWYBRW-UMQVHGATSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
METHYL-2,3,4-TRI-O-ACETYL-6-O-(2',3',4'-TRI-O-ACETYL-6',7'-DIDEOXY-BETA-D-GALACTO-HEPTOPYRANOSYL)-ALPHA-D-GALACTOPYRANOSIDE
ZXKLNSRPHLJLBU-GVALYFOVSA-N
METHYL-4-O-BENZOYL-2,6-DIDEOXY-3-O-METHYL-ALPHA-L-RIBO-HEXOPYRANOSYL-(1->6)-2,3,4-TRI-O-ACETYL-ALPHA-D-GLUCOPYRANOSIDE
METHYL 2,3-DI-O-ACETYL-4-O-(2,3,4,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSYL)-BETA-D-XYLOPYRANOSIDE
METHYL 2,3-DI-O-ACETYL-4-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-BETA-D-XYLOPYRANOSIDE
METHYL 2,3-DI-O-ACETYL-4-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL)-BETA-D-XYLOPYRANOSIDE
METHYL 2,3-DI-O-ACETYL-4-O-(2,3,4,6-TETRA-O-ACETYL-ALPHA-D-GALACTOPYRANOSYL)-BETA-D-XYLOPYRANOSIDE
RHODIOOCTANOSIDE_HEXAACETATE
UZEDMSSSHUUMFP-YLKNCTOASA-N
ISOCLATHROSIDE_A_PERACETATE
| Title | Journal or Book | Year |
|---|---|---|
| Convenient, in Situ Generation of Anhydrous Hydrogen Iodide for the Preparation of α-Glycosyl Iodides and Vicinal Iodohydrins and for the Catalysis of Ferrier Glycosylation | Organic Letters | 2000 |