5-[(1S,2S,Z)-1,2-(ETHYLIDENEDIOXY)-HEX-3-ENYL]-2,2-BIS-(HYDROXYMETHYL)-4-METHYLFURAN-3(2H)-ONE
Compound with spectra: 1 NMR
![5-[(1S,2S,Z)-1,2-(ETHYLIDENEDIOXY)-HEX-3-ENYL]-2,2-BIS-(HYDROXYMETHYL)-4-METHYLFURAN-3(2H)-ONE](/api/compound/57hyxt7hw9J.png?ph=true&h=300&w=458 "5-[(1S,2S,Z)-1,2-(ETHYLIDENEDIOXY)-HEX-3-ENYL]-2,2-BIS-(HYDROXYMETHYL)-4-METHYLFURAN-3(2H)-ONE")
| SpectraBase Compound ID | 57hyxt7hw9J |
|---|---|
| InChI | InChI=1S/C15H22O6/c1-4-5-6-11-13(20-10(3)19-11)12-9(2)14(18)15(7-16,8-17)21-12/h5-6,10-11,13,16-17H,4,7-8H2,1-3H3/b6-5-/t10?,11-,13-/m0/s1 |
| InChIKey | JXLGQZKRYNETNG-CLTNUMGLSA-N |
| Mol Weight | 298.34 g/mol |
| Molecular Formula | C15H22O6 |
| Exact Mass | 298.141638 g/mol |
| Enantiomer InChIKey | JXLGQZKRYNETNG-ZLHWPBJISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
Ethyl 2,6-anhydro-3-deoxy-8,9-O-isopropylidene-7-O-(methoxymethyl)-D-glycero-D-talo-non-4-ulosonate
1,2:4,5-di-O-cyclohexyliden-3-O-methyl-1,2-didehydro-D-arabino-hexitol
(4Z)-(1S,2R,6R,7AR,7BR)-7A,7B-DIMETHOXY-2-METHOXYMETHYLHYDROXY-7A,7B-DIMETHYL-7,8-DIOXA-BICYCLO-[4.4.0]-DEC-4-ENE
tert-Butyl 4-{5(S)-[5(S)-hydroxy-4(R)-methylhex-2(E)-enyl]-3(S),4(R)-(cyclohexylidenedioxy)tetrahydropyran-2(S)-yl}-3-methyl-2(E)-butenoate
2-HYDROXY-3-DEOXY-5,6:7,8-DI-O-ISOPROPYLIDENE-D-MANNO-2-OCTENO-1,4-LACTONE
PHENYL-2,3,4,6-TETRA-O-BENZYL-1-SELENO-BETA-D-GLUCOPYRANOSIDE
[1(1')Z]-2,3,4-TRI-O-BENZYL-1-DEOXY-6-O-(PARA-METHOXYBENZYL)-1-PROPYLIDENE-D-MANNOPYRANOSIDE
PARA-NITROPHENYL 6-O-(ALPHA-D-MANNOPYRANOSYLPHOSPHO)-BETA-D-GLUCOPYRANOSIDE, TRIETHYLAMMONIUM SALT
N-ACETYL-AUREOTHAMINE
3-O-(1,3-PROPYLENDIOXYTHIOPHOSPHORYL)-5,6-O-ISOPROPYLIDENE-L-ASCORBINIC ACID
| Title | Journal or Book | Year |
|---|---|---|
| Synthetic studies directed toward the pseurotins. Part II. Synthesis of related highly functionalized furan-3(2H)-ones | Helvetica Chimica Acta | 1990 |