(2E,4R,5S,6S,15R)-4,5-EPOXY-6-[[(IMIDAZOL-1-YL)-THIOCARBONYL]-OXY]-HEXADEC-2-EN-15-OLIDE
Compound with spectra: 1 NMR
![(2E,4R,5S,6S,15R)-4,5-EPOXY-6-[[(IMIDAZOL-1-YL)-THIOCARBONYL]-OXY]-HEXADEC-2-EN-15-OLIDE](/api/compound/HLZp4LI4r57.png?ph=true&h=300&w=458 "(2E,4R,5S,6S,15R)-4,5-EPOXY-6-[[(IMIDAZOL-1-YL)-THIOCARBONYL]-OXY]-HEXADEC-2-EN-15-OLIDE")
| SpectraBase Compound ID | HLZp4LI4r57 |
|---|---|
| InChI | InChI=1S/C20H28N2O4S/c1-15-8-6-4-2-3-5-7-9-16(26-20(27)22-13-12-21-14-22)19-17(25-19)10-11-18(23)24-15/h10-17,19H,2-9H2,1H3/b11-10+/t15-,16+,17-,19+/m1/s1 |
| InChIKey | BGPOJNRZDYZOGA-XPPFYOFMSA-N |
| Mol Weight | 392.51 g/mol |
| Molecular Formula | C20H28N2O4S |
| Exact Mass | 392.176979 g/mol |
| Enantiomer InChIKey | BGPOJNRZDYZOGA-IHSWYFQTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(Z)-ETHYL-1,2,6,7-TETRADEOXY-3,4-ISOPROPYLIDENE-D-LYXO-OCTA-1,6-DIENO-1,5-PYRANOSURONATE
SAOIZPQPDPYLCN-CMADAAASSA-N
8,9-EPOXYCINEROMYCIN;SECOND-DIASTEREOISOMER
8,9-EPOXYCINEROMYCIN;ONE-DIASTEREOISOMER
RAMARIOLIDE_B
(E,5R,6R)-5-[3-[(4S,5S)-2,2-dimethyl-5-vinyl-1,3-dioxolan-4-yl]propanoyloxy]-6-(methoxymethoxy)dodec-2-enoic acid methyl ester
(2R)-2-[(1R,2S)-1-benzoxy-2-hydroxy-2-phenyl-ethyl]-2,3-dihydropyran-6-one
(2R,5R,6R,7S)-Germacra-1(10)E,4(15)-dien-5-hydroperoxy-2,6-diol-2-acetate
(2R,3S,2'S,2''S,4''AR,8''AS)-2-[2'-(2'',4''A,6'',7'',8'',8''A)-HEXAHYDROPYRAN-[3,2-B]-PYRAN-2''-YL-2'-HYDROXYETHYL]-TETRAHYDROPYRAN-3-OL
| Title | Journal or Book | Year |
|---|---|---|
| Synthese des Makrolid-Antibiotikums (−)-A26771B mit Photolactonisierung als Schlüsselreaktion und Computersimulation als effektive Optimierungshilfe | Helvetica Chimica Acta | 1991 |