(1R)-4-(tert-butyl-di(phenyl)silyl)oxy-1-[(2R,5S)-5-[(1S)-4-(tert-butyl-di(phenyl)silyl)oxy-1-hydroxybutyl]oxolan-2-yl]butan-1-ol
Compound with spectra: 1 NMR
![(1R)-4-(tert-butyl-di(phenyl)silyl)oxy-1-[(2R,5S)-5-[(1S)-4-(tert-butyl-di(phenyl)silyl)oxy-1-hydroxybutyl]oxolan-2-yl]butan-1-ol](/api/compound/3774PivrZny.png?ph=true&h=300&w=458 "(1R)-4-(tert-butyl-di(phenyl)silyl)oxy-1-[(2R,5S)-5-[(1S)-4-(tert-butyl-di(phenyl)silyl)oxy-1-hydroxybutyl]oxolan-2-yl]butan-1-ol")
| SpectraBase Compound ID | 3774PivrZny |
|---|---|
| InChI | InChI=1S/C44H60O5Si2/c1-43(2,3)50(35-21-11-7-12-22-35,36-23-13-8-14-24-36)47-33-19-29-39(45)41-31-32-42(49-41)40(46)30-20-34-48-51(44(4,5)6,37-25-15-9-16-26-37)38-27-17-10-18-28-38/h7-18,21-28,39-42,45-46H,19-20,29-34H2,1-6H3/t39-,40+,41-,42+ |
| InChIKey | ANWQIBGEOJZKFH-LDCYWHLHSA-N |
| Mol Weight | 725.1 g/mol |
| Molecular Formula | C44H60O5Si2 |
| Exact Mass | 724.397928 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
6-Allyl-1-[3'-(tert-butyldiphenylsilyl)propyl]-1,2,3,6-tetradeoxy-.alpha.,D-erythro-hexopyranose
1-[3'-(tert-Butyldiphenylsilyl)propyl]-1,2,3-trideoxy-.alpha.,D-erythro-hexopyranose
2,2,5-Trimethyl-5-[4-(tert-butyldiphenylsilyloxy)butyl]-1,3-dioxolane
11-[(t-Butyldiphenyl)silanyloxy]-1-(4'-methoxyphenyl)methoxy]undecane-4,5-dione - dioxime
(2S,5S)-2-n-Butyl-5-(tert-butyldiphenylsiloxymethyl)tetrahydrofuran
(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE
6-[(tert-Butyldiphenylsilyloxy)ethyl]-5-methyl-3,4,5,6-tetrahydropyran-2-one
Ethyl (2R,3R,5S)-7-((tert-butyldiphenylsilyl)oxy)-3-hydroxy-2,5-dimethylheptanoate
6-[3-(TERT.-BUTYLDIPHENYLSILYLOXY)-PROPYL]-2-METHYLPYRIDAZIN-3(2H)-ONE
5-[tert-butyl(diphenyl)silyl]oxy-2,2-dimethyl-3-oxopentanoic acid ethyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Total Synthesis of cis-Solamin: Exploiting the RuO4-Catalyzed Oxidative Cyclization of Dienes | Organic Letters | 2006 |