MAJOR-ENANTIOMER
Compound with spectra: 2 NMR
| SpectraBase Compound ID | 2SXV7NsryO0 |
|---|---|
| InChI | InChI=1S/C30H43F3O5Si/c1-18(2)39(19(3)4,20(5)6)38-28-17-16-23-24(14-15-25(37-28)26(23)21(28)7)36-27(34)29(35-8,30(31,32)33)22-12-10-9-11-13-22/h9-15,18-21,23-26H,16-17H2,1-8H3/t21-,23-,24-,25+,26-,28+,29?/m1/s1 |
| InChIKey | MRQLNAZDYHGCEU-HYFHEUTMSA-N |
| Mol Weight | 568.7 g/mol |
| Molecular Formula | C30H43F3O5Si |
| Exact Mass | 568.283186 g/mol |
| Enantiomer InChIKey | MRQLNAZDYHGCEU-ACQXGXFASA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- MINOR-ENANTIOMER
QUERCETIN-3-O-(2''-ACETYL)-BETA-D-GALACTOSIDE
ENT-7-BETA,12-ALPHA-DIHYDROXY-3-OXO-13-EPI-MANOYL-OXIDE
METHYL-ENT-15-OXO-KAUR-16-EN-19-OATE
METHYL-2-OXO-6-ALPHA,15-DIACETOXY-8-ALPHA-(PARA-ACETOXYPHENYLACETOXY)-GUAIA-1(10),3,11-TRIEN-5-ALPHA-H-12-OATE
METHYL-2-OXO-6A,15-DIACETOXY-8A-(P-ACETOXYPHENYLACETOXY)-GUAIA-1(10),3,11-TRIEN-5AH-12-OATE
2,2-Hydroxymethylene-androsta-3,5-diene-3,17.beta.-diol, O',O'',O'''-tris-TMS
.alpha.-D-Glucopyranoside, 1,3,4,6-tetrakis-o-(2,2-dimethyl-1-oxopropyl)-.beta.-D-fructofuranosyl, 3,4,6-tris(2,2-dimethylpropanoate)
9-ALPHA-HYDROXY-LEUCODIN-9-O-BETA-XYLOPYRANOSIDE
Methyl 4-(ethylene-1',2'-dioxy)-8-[(t-butyldimethylsilyl)oxy]-1,5-dioxo-(decahydro)naphthalene-10-carboxylate
Triacetyl-oleandomylin
| Title | Journal or Book | Year |
|---|---|---|
| Application of Chiral Cationic Catalysts to Several Classical Syntheses of Racemic Natural Products Transforms Them into Highly Enantioselective Pathways | Journal of the American Chemical Society | 2004 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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