#11;[3AR-(3A-ALPHA,4-ALPHA,5-ALPHA,7A-ALPHA)]-6-BROMO-2,2-DIMETHYL-4,5-BIS-(3-PHENYL-(E)-2-PROPENYLOXY)-3A,4,5,7A-TETRAHYDRO-2,2-DIMETHYL-1,3-BENZODIOXOLE
Compound with spectra: 1 NMR
![#11;[3AR-(3A-ALPHA,4-ALPHA,5-ALPHA,7A-ALPHA)]-6-BROMO-2,2-DIMETHYL-4,5-BIS-(3-PHENYL-(E)-2-PROPENYLOXY)-3A,4,5,7A-TETRAHYDRO-2,2-DIMETHYL-1,3-BENZODIOXOLE](/api/compound/LLnlPXQ9Miu.png?ph=true&h=300&w=458 "#11;[3AR-(3A-ALPHA,4-ALPHA,5-ALPHA,7A-ALPHA)]-6-BROMO-2,2-DIMETHYL-4,5-BIS-(3-PHENYL-(E)-2-PROPENYLOXY)-3A,4,5,7A-TETRAHYDRO-2,2-DIMETHYL-1,3-BENZODIOXOLE")
| SpectraBase Compound ID | LLnlPXQ9Miu |
|---|---|
| InChI | InChI=1S/C27H29BrO4/c1-27(2)31-23-19-22(28)24(29-17-9-15-20-11-5-3-6-12-20)26(25(23)32-27)30-18-10-16-21-13-7-4-8-14-21/h3-16,19,23-26H,17-18H2,1-2H3/b15-9+,16-10+/t23-,24-,25-,26-/m1/s1 |
| InChIKey | VEYVGWGDKOAPHU-NNSGEEMQSA-N |
| Mol Weight | 497.43 g/mol |
| Molecular Formula | C27H29BrO4 |
| Exact Mass | 496.124922 g/mol |
| Enantiomer InChIKey | VEYVGWGDKOAPHU-AKESRFQASA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3R,4R,5R,6R)-1-Chloro-3,4:5,6-bis(isopropylidenedioxy)cyclohex-1-ene
(4S,5R,6S,7S)-4,5:6,7-BIS-(IOSPROPYLIDENEDIOXY)-2-CYCLOHEPTEN-1-ONE
(3aR,4R,5R,7aR)-4-methoxy-2,2-dimethyl-7-(7-methyl-3-methylene-oct-6-en-1-ynyl)-3a,4,5,7a-tetrahydro-1,3-benzodioxol-5-ol
ETHYL-TRANS-2,3-DIDEOXY-4,5:7,8-DI-O-ISOPROPYLIDENE-6-O-TERT.-BUTYL-DIMETHYLSILYL-D-GLUCO-2-OCTONENATE
[(3aR,5aS,6aS,6bR)-5-spiro[3a,5a,6a,6b-tetrahydrooxireno[2,3-g][1,3]benzodioxole-2,1'-cyclohexane]yl]methanol
2-HYDROXY-3-DEOXY-5,6:7,8-DI-O-ISOPROPYLIDENE-D-MANNO-2-OCTENO-1,4-LACTONE
5-Desoxy-1,2-O-isopropylidene-5-C-methylene-A-D-xylo-hexofuranurono-6,3-lactone
(2R,3R,4R,5R)-(-)-1,2:4,5-Di(isopropylidenedioxy)hept-6-en-3-yl p-toluenesulfonate
6-DEOXY-1,2:3,4-DI-O-ISOPROPYLIDENE beta(L) ARABINO-HEX-5-ENOPYRANOSE
.alpha.-D-Galactohex-5-enopyranose, 1,2:3,4-di-O-isopropylidene-5,6-dideoxy-
| Title | Journal or Book | Year |
|---|---|---|
| Use of Electrochemical Methods as an Alternative to Tin Reagents for the Reduction of Vinyl Halides in Inositol Synthons | The Journal of Organic Chemistry | 1999 |