benzoic acid [(1R,2R,3R,4R,5S)-2-(benzyloxy)-5-(dimethoxymethyl)-4-(2-ethoxy-2-keto-ethyl)-3-hydroxy-cyclopentyl] ester
Compound with spectra: 1 NMR
![benzoic acid [(1R,2R,3R,4R,5S)-2-(benzyloxy)-5-(dimethoxymethyl)-4-(2-ethoxy-2-keto-ethyl)-3-hydroxy-cyclopentyl] ester](/api/compound/BjV65LZiajr.png?ph=true&h=300&w=458 "benzoic acid [(1R,2R,3R,4R,5S)-2-(benzyloxy)-5-(dimethoxymethyl)-4-(2-ethoxy-2-keto-ethyl)-3-hydroxy-cyclopentyl] ester")
| SpectraBase Compound ID | BjV65LZiajr |
|---|---|
| InChI | InChI=1S/C26H32O8/c1-4-32-20(27)15-19-21(26(30-2)31-3)23(34-25(29)18-13-9-6-10-14-18)24(22(19)28)33-16-17-11-7-5-8-12-17/h5-14,19,21-24,26,28H,4,15-16H2,1-3H3/t19-,21+,22-,23-,24-/m1/s1 |
| InChIKey | GZWNLMSBKWBVOQ-DXVXXHEXSA-N |
| Mol Weight | 472.5 g/mol |
| Molecular Formula | C26H32O8 |
| Exact Mass | 472.209718 g/mol |
| Enantiomer InChIKey | GZWNLMSBKWBVOQ-FGQYTZQDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2-O-BENZOYL-3,4-DI-O-BENZYL-ALPHA-L-RHAMNOPYRANOSYL-TRICHLOROACETIMIDATE
ETHYL-2-O-BENZOYL-3,6-DI-O-BENZYL-1-THIO-BETA-D-GLUCOPYRANOSIDE
BENZYL-6-O-(4-METHOXYBENZYL)-2,3-DI-O-BENZOYL-BETA-D-GLUCOPYRANOSIDE
ZEYLENOL-EPOXIDE
(3R,5R,6S,7R)-6,7-Dibenzyloxy-3-methoxy-5-nitro-2-oxabicyclo[2.2.1]heptane
Methyl 2,6-di-O-benzyl-3,4-bis(O-[4-bromo-benzoyl]).alpha.-D-galactopyranoside
(3S)-3-HYDROXY-(6R)-6-(2,3,5-TRI-O-BENZOYL-BETA-D-RIBOFURANOSYL)-2,3-DIHYDRO-6H-PYRAN
2,3,4-TRI-O-BENZOYL-ALPHA-D-MANNOPYRANOSYLHYDROGENPHOSPHONATE,TRIETHYLAMMONIUM SALT
5-(METHOXYCARBONYL)-PENTYL-2-O-BENZOYL-3,6-DI-O-BENZYL-4-O-METHYL-BETA-D-GALACTOPYRANOSIDE
METHYL-2,3-DI-O-BENZOYL-4-FLUORO-ALPHA-D-GLUCOPYRANUROIC-ACID
| Title | Journal or Book | Year |
|---|---|---|
| Radical cyclization routes to bridged pyranosides as precursors of densely functionalized cycloalkanes | The Journal of Organic Chemistry | 1992 |