(2Z,4E,6S,15R)-6-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-HEXADECA-2,4-DIEN-15-OLIDE
Compound with spectra: 1 NMR
![(2Z,4E,6S,15R)-6-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-HEXADECA-2,4-DIEN-15-OLIDE](/api/compound/7A6BbxcXLxJ.png?ph=true&h=300&w=458 "(2Z,4E,6S,15R)-6-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-HEXADECA-2,4-DIEN-15-OLIDE")
| SpectraBase Compound ID | 7A6BbxcXLxJ |
|---|---|
| InChI | InChI=1S/C22H40O3Si/c1-19-15-11-9-7-8-10-12-16-20(17-13-14-18-21(23)24-19)25-26(5,6)22(2,3)4/h13-14,17-20H,7-12,15-16H2,1-6H3/b17-13+,18-14-/t19-,20+/m1/s1 |
| InChIKey | DXLHXEHJJILKGD-QTSPIXMESA-N |
| Mol Weight | 380.6 g/mol |
| Molecular Formula | C22H40O3Si |
| Exact Mass | 380.274672 g/mol |
| Enantiomer InChIKey | DXLHXEHJJILKGD-AGFVMQINSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
tert-Butyl-dimethyl-[(E)-1-tributylstannyloct-1-en-3-yl]oxy-silane
Methyl 15-methoxy-9,16-bis(trimethylsilyloxy)-octadeca-10,12-dienoate
(5E,8R,14R)-14-amyl-8-[tert-butyl(dimethyl)silyl]oxy-1-oxacyclotetradec-5-en-2-one
(E)-(8S,14R)-8-(tert-Butyl-dimethyl-silanyloxy)-14-pentyl-oxacyclotetradec-5-en-2-one
(8R,14R)-8-(T-Butyl-dimethyl-silyloxy)-2-oxo-14-pentyl-trans-1-oxa-cyclotetradec-5-ene
2-Cyclopenten-1-ol, 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, acetate, (1R-trans)-
N1-[(2R,3E,5E)-7-Hydroxy-2-methyl-3,5-heptadienyl]-(2E,4E,6E,9S,10E)-9-{[1-(tert-butyl)-1,1-dimethylsilyl]oxy}-12-hydroxy-2,4,6,10-dodecatetraenamide
tert-Butyl(((2R,4S,Z)-2-(butylthio)dec-5-en-4-yl)oxy)dimethylsilane
(+)-(3S,4S,6E,9R,10E)-3,9-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-4-METHYLDODECA-6,10-DIEN-1-OL
| Title | Journal or Book | Year |
|---|---|---|
| Synthese des Makrolid-Antibiotikums (−)-A26771B mit Photolactonisierung als Schlüsselreaktion und Computersimulation als effektive Optimierungshilfe | Helvetica Chimica Acta | 1991 |