METHYL-(2'R,3'R,4'R,5'R)-2-[(Z)-2'-(4-FLUOROPHENYL)-VINYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE
Compound with spectra: 1 NMR
![METHYL-(2'R,3'R,4'R,5'R)-2-[(Z)-2'-(4-FLUOROPHENYL)-VINYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE](/api/compound/3NzzPL6Nylm.png?ph=true&h=300&w=458 "METHYL-(2'R,3'R,4'R,5'R)-2-[(Z)-2'-(4-FLUOROPHENYL)-VINYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE")
| SpectraBase Compound ID | 3NzzPL6Nylm |
|---|---|
| InChI | InChI=1S/C18H21FO5/c1-18(2)23-16-13(10-15(20)21-3)14(22-17(16)24-18)9-6-11-4-7-12(19)8-5-11/h4-9,13-14,16-17H,10H2,1-3H3/b9-6-/t13-,14-,16-,17-/m1/s1 |
| InChIKey | HZJFGEPHRXIDHJ-SZJUXVHMSA-N |
| Mol Weight | 336.36 g/mol |
| Molecular Formula | C18H21FO5 |
| Exact Mass | 336.137302 g/mol |
| Enantiomer InChIKey | HZJFGEPHRXIDHJ-YSRHVXHDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
METHYL-(2'R,3'R,4'R,5'R)-2-[2'-(4-FLUOROPHENYL)-ETHYL-4',5'-ISOPROPYLIDENE-DIOXY-TETRAHYDRO-FURAN-3'-YL]-ACETATE
6-Bromo-3,6-dideoxy-3-C-(methoxycarbonylmethyl)-1,2-O-isopropylidene-.alpha.-D-allofuranose
6-Bromo-3,6-dideoxy-3-C-[(E)-(methoxycarbonyl)-2-propenyl]-1,2-O-isopropylidene-.alpha.-D-allofuranose
3-O-BENZYL-5,6,8-TRIDEOXY-7-HYDROXYIMINO-1,2-O-ISOPROPYLIDENE-ALPHA-D-RIBO-OCT-5-(E)-ENFURANOSE
3-O-BENZYL-5,6,8-TRIDEOXY-7-HYDROXYIMINO-1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLO-OCT-5-(E)-ENFURANOSE
.alpha.-D-Allofuranose, 5,6-anhydro-3-deoxy-3-[[(4-methoxyphenyl)methoxy]methyl]-1,2-O-(1-methylethylidene)-
TERT.-BUTYL-(E)-3-(6-BENZYLOXY-2,2-DIMETHYLTETRAHYDRO-FURO-[2,3-D]-[1,3]-DIOXOL-5-YL)-ACRYLATE
.alpha.-D-Allofuranose, 3,5-dideoxy-6-O-[(4-methoxyphenyl)methyl]-5-methyl-1,2-O-(1-methylethylidene)-3-[(phenylmethoxy)methyl]-
.alpha.-D-Allofuranose, 3,5-dideoxy-5-(hydroxymethyl)-3-[[(4-methoxyphenyl)methoxy]methyl]-1,2-O-(1-methylethylidene)-6-O-(phenylmethyl)-
.beta.-L-Talofuranose, 3,5-dideoxy-3-[[(4-methoxyphenyl)methoxy]methyl]-5-methyl-1,2-O-(1-methylethylidene)-6-O-(phenylmethyl)-
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis and antifungal activity of halogenated aromatic bis-γ-lactones analogous to avenaciolide | Química Nova | 2012 |