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 © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- MINOR-ENANTIOMER
7,7-Difluoro-6-(propenyl)-8-phenyl-5,10-dioxa-8-azabenzo[c]bicyclo[3.2.1]octane
Pregn-5-ene-21-carboxylic acid, 17-hydroxy-3-[(trimethylsilyl)oxy]-, .gamma.-lactone, (3.beta.,17.alpha.)-
QUERCETIN-3-O-(2''-ACETYL)-BETA-D-GALACTOSIDE
ENT-7-BETA,12-ALPHA-DIHYDROXY-3-OXO-13-EPI-MANOYL-OXIDE
Ethyl 5-methyl-1-phenyl-3-(7-phenyl-7H-thiazolo[3,2-a]pyrimidin-5-yl)-1H-pyrazole-4-carboxylate
METHYL-2-OXO-6-ALPHA,15-DIACETOXY-8-ALPHA-(PARA-ACETOXYPHENYLACETOXY)-GUAIA-1(10),3,11-TRIEN-5-ALPHA-H-12-OATE
Acetic acid, [7-(acetyloxy)-8-formyldodecahydro-10-hydroxy-1,4b,8-trimethyl-2(1H)- phenanthrenylidene]-, 2-(methylamino)ethyl ester, hydrochloride, [1R-(1.alpha.,2E,4a.alpha.,4b.beta.,7.beta.,8.beta.,8a.alpha.,10.beta.,10a.beta.)]-
ethyl 2-{6-[(3-chloro-4-methoxyphenyl)carbamoyl]-4-oxo-10-oxa-3-azatricyclo[5.2.1.0¹,⁵]dec-8-en-3-yl}acetate
2H-indol-2-one, 5-chloro-3-[2-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-oxoethyl]-1,3-dihydro-3-hydroxy-1-(2-thienylmethyl)-
.alpha.-D-Glucopyranoside, 1,3,4,6-tetrakis-O-(2,2-dimethyl-1-oxopropyl)-.beta.-D-fructofuranosyl, 3,4,6-tris(2,2-dimethylpropanoate)
| 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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