(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-3-IODO-2-METHOXY-HEXAHYDROFURO-[3,2-B]-FURAN;METHYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA-D-GLUCOFURANOSIDE
Compound with spectra: 1 NMR
![(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-3-IODO-2-METHOXY-HEXAHYDROFURO-[3,2-B]-FURAN;METHYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA-D-GLUCOFURANOSIDE](/api/compound/AnDV6XMr4N3.png?ph=true&h=300&w=458 "(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-3-IODO-2-METHOXY-HEXAHYDROFURO-[3,2-B]-FURAN;METHYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA-D-GLUCOFURANOSIDE")
| SpectraBase Compound ID | AnDV6XMr4N3 |
|---|---|
| InChI | InChI=1S/C14H17IO4/c1-16-14-11(15)13-12(19-14)10(8-18-13)17-7-9-5-3-2-4-6-9/h2-6,10-14H,7-8H2,1H3/t10-,11-,12-,13-,14-/m1/s1 |
| InChIKey | FOCSXMHEVUFHEO-DHGKCCLASA-N |
| Mol Weight | 376.19 g/mol |
| Molecular Formula | C14H17IO4 |
| Exact Mass | 376.017154 g/mol |
| Enantiomer InChIKey | FOCSXMHEVUFHEO-PEDHHIEDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Benzyl 6-O-Benzyl-3,5-di-O-methyl-.alpha.,D-glucofuranoside
METHYL-2,3,4-TRI-O-BENZYL-6-DEOXY-ALPHA-L-ALTROPYRANOSIDE
Methyl 2-O-methyl-3,4-di-O-benzyl.alpha.-L-rhamnopyranoside
Methyl 2,4-di-O-benzyl-3-O-methyl.alpha.-L-rhamnopyranoside
Methyl 2,3-di-O-benzyl-6-deoxy-4-O-methylhexopyranoside
Methyl 2,3-di-O-benzyl-4-O-methyl.alpha.-L-rhamnopyranoside
METHYL-4,6-DI-O-BENZYL-ALPHA-D-TALOPYRANOSIDE
Methyl 5-O-acetyl-2,3,6-tri-O-methylhexofuranoside
1,2,4-O-Tribenzyl-.beta.,D-arabinopyranose-3-O-formyl
1,2,4-O-Tribenzyl-.beta.,D-arabinopyranose-3-carboxylic acid isomer
| Title | Journal or Book | Year |
|---|---|---|
| Iodoetherification of Isosorbide-Derived Glycals: Access to a Variety ofO-Alkyl orO-Aryl Isosorbide Derivatives | European Journal of Organic Chemistry | 2013 |