10-(TERT.-BUTYLDIMETHYLSILOXY)-12-(TERT.-BUTYLDIMETHYLSILYL)-13-HYDROXY-8-OXA-TRICYCLO-[7.3.2.0(7,2)]-TETRADEC-10-EN-14-ONE
Compound with spectra: 1 NMR
![10-(TERT.-BUTYLDIMETHYLSILOXY)-12-(TERT.-BUTYLDIMETHYLSILYL)-13-HYDROXY-8-OXA-TRICYCLO-[7.3.2.0(7,2)]-TETRADEC-10-EN-14-ONE](/api/compound/IFcijQqaicy.png?ph=true&h=300&w=458 "10-(TERT.-BUTYLDIMETHYLSILOXY)-12-(TERT.-BUTYLDIMETHYLSILYL)-13-HYDROXY-8-OXA-TRICYCLO-[7.3.2.0(7,2)]-TETRADEC-10-EN-14-ONE")
| SpectraBase Compound ID | IFcijQqaicy |
|---|---|
| InChI | InChI=1S/C25H46O4Si2/c1-24(2,3)30(7,8)19-15-18(29-31(9,10)25(4,5)6)23-22(27)21(26)20(19)16-13-11-12-14-17(16)28-23/h15-17,19-21,23,26H,11-14H2,1-10H3/t16-,17-,19+,20-,21?,23+/m1/s1 |
| InChIKey | BPQXJMKQZDWKEU-KJSHWPJLSA-N |
| Mol Weight | 466.8 g/mol |
| Molecular Formula | C25H46O4Si2 |
| Exact Mass | 466.293463 g/mol |
| Enantiomer InChIKey | BPQXJMKQZDWKEU-GWNFALGVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N-Cyano-16(R)-cyano-16-decarbomethoxy-19,20(S)-dihydro-15(R)-hydroxyperivine
JLLATAGHVXJXGR-KGPPGCELSA-N
(2S,2'R,3R/S)-2-[2-Hydroxyperoxy-3-(phenylsulfonyl)propyl]-5.alpha.-cholestan-3-one 2',3-peroxyhemiacetal
1,2,2a,3,4,5,Hexahydro-2a,8-dimethoxy-1,5-dimethyl-2-oxopyrrolo[4,3,2-de]quinoline
2-BETA,3-BETA-DIHYDROXY-6-(E)-HYDROXIMINO-CHOLEST-4-ENE
(2S,3R,6E,8S,9S,10R,13R,14S,17R)-6-hydroxyimino-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-2,3-diol
2-ALPHA,3-ALPHA-DIHYDROXY-6-(E)-HYDROXIMINO-CHOLEST-4-ENE
6,8-DIHYDRO-8-(HYDROXYMETHYL)-1-INDANYL-1'-BETA-D-GLUCOPYRANOSIDE-HEPTAACETATE
GLAUCOPINE_B;14-HYDROXY-11-METHOXY-8-OXOCYATHA-3,12-DIENE-12-CARBALDEHYDE
MAMMEA-E/BD-CYCLO-D
| Title | Journal or Book | Year |
|---|---|---|
| Stereoselective Construction of Eight-Membered Oxygen Heterocycles by Brook Rearrangement-Mediated [3 + 4] Annulation | Organic Letters | 2004 |