(2Z,4S,5S,6S,15R)-6-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-4,5-EPOXYHEXADEC-2-EN-15-OLIDE
Compound with spectra: 1 NMR
![(2Z,4S,5S,6S,15R)-6-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-4,5-EPOXYHEXADEC-2-EN-15-OLIDE](/api/compound/HxN3Lg5ZhEv.png?ph=true&h=300&w=458 "(2Z,4S,5S,6S,15R)-6-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-4,5-EPOXYHEXADEC-2-EN-15-OLIDE")
| SpectraBase Compound ID | HxN3Lg5ZhEv |
|---|---|
| InChI | InChI=1S/C22H40O4Si/c1-17-13-11-9-7-8-10-12-14-19(26-27(5,6)22(2,3)4)21-18(25-21)15-16-20(23)24-17/h15-19,21H,7-14H2,1-6H3/b16-15-/t17-,18-,19+,21-/m1/s1 |
| InChIKey | JGJZASWIPAVXSF-ZSZBGBDGSA-N |
| Mol Weight | 396.6 g/mol |
| Molecular Formula | C22H40O4Si |
| Exact Mass | 396.269586 g/mol |
| Enantiomer InChIKey | JGJZASWIPAVXSF-MWTQOHAPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2E,4S,5S,6S,15R)-4-HYDROXY-5,6-(ISOPROPYLIDENDIOXY)-HEXADEC-2-EN-15-OLIDE
(2Z,4S,5S,6S,15R)-4,5-(CARBONYLDIOXY)-6-HYDROXYHEXADEC-2-EN-15-OLIDE
(2E,4S,5S,6S,15R)-4,5-(CARBONYLDIOXY)-5-HYDROXYHEXADEC-2-EN-15-OLIDE
(2E,4R,5S,6S,15R)-4,5-(CARBONYLDIOXY)-6-HYDROXYHEXADEC-2-EN-15-OLIDE
(2R,3R,8R)-3-((tert-Butyldimethylsilyl)oxy)-2-ethyl-8-(2-(methoxycarbonyl)vinyl)-3,4,7,8-tetrahydro-2H-oxocin
(1SR,4S,5S)-1-Acetoxy-5-tert-butyldimethylsilyloxy-1,4-epoxyheptadecane
(2E,4R,5S,11R)-4,5-bis[(1',1'-Dimethylethyl)dimethylsilyloxy]-11-hydroxy-2-dodecenoic acid - Methyl ester
| Title | Journal or Book | Year |
|---|---|---|
| Synthese des Makrolid-Antibiotikums (−)-A26771B mit Photolactonisierung als Schlüsselreaktion und Computersimulation als effektive Optimierungshilfe | Helvetica Chimica Acta | 1991 |