(2Z,4E,6R,15R)-6-HYDROXYHEXADECA-2,4-DIEN-15-OLIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Dqod8bvW62X |
|---|---|
| InChI | InChI=1S/C16H26O3/c1-14-10-6-4-2-3-5-7-11-15(17)12-8-9-13-16(18)19-14/h8-9,12-15,17H,2-7,10-11H2,1H3/b12-8+,13-9-/t14-,15-/m1/s1 |
| InChIKey | YUINNLXMFSWVJE-HMWZSIAFSA-N |
| Mol Weight | 266.38 g/mol |
| Molecular Formula | C16H26O3 |
| Exact Mass | 266.188195 g/mol |
| Enantiomer InChIKey | YUINNLXMFSWVJE-PWSULBMRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2E,4S,12R)-4-HYDROXY-2-TRIDECEN-12-OLIDE;(E)-HOMOPATULOLIDE_C
(2Z,4S,12R)-4-HYDROXY-2-TRIDECEN-12-OLIDE;(Z)-HOMOPATULOLIDE_C
(2E,4S,11R)-4-HYDROXY-2-DODECEN-11-OLIDE;(E)-PATULOLIDE_C
(2Z,4S,11R)-4-HYDROXY-2-DODECEN-11-OLIDE;(Z)-ISOPATULOLIDE_C
(2Z,4S,10R)-4-HYDROXY-2-UNDECEN-10-OLIDE;(Z)-NORISOPATULOLIDE_C
| Title | Journal or Book | Year |
|---|---|---|
| Synthese des Makrolid-Antibiotikums (−)-A26771B mit Photolactonisierung als Schlüsselreaktion und Computersimulation als effektive Optimierungshilfe | Helvetica Chimica Acta | 1991 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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