(2E,4R,5S,6S,15R)-4,5-EPOXY-6-(TOSYLOXY)-HEXADEC-2-EN-15-OLIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | D82OB7mOqSo |
|---|---|
| InChI | InChI=1S/C23H32O6S/c1-17-11-13-19(14-12-17)28-30(25)29-21-10-8-6-4-3-5-7-9-18(2)26-22(24)16-15-20-23(21)27-20/h11-16,18,20-21,23H,3-10H2,1-2H3/b16-15+/t18-,20-,21+,23-,30?/m1/s1 |
| InChIKey | XKWNPBYDUDHMMW-OUTMLWBASA-N |
| Mol Weight | 436.6 g/mol |
| Molecular Formula | C23H32O6S |
| Exact Mass | 436.19196 g/mol |
| Enantiomer InChIKey | XKWNPBYDUDHMMW-GGPHXNBKSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2E,4S,5S,6S,15R)-6-HYDROXY-4,5-(ISOPROPYLIDENDIOXY)-HEXADEC-2-EN-15-OLIDE
(3E,5R,6S,12R)-5,6-bis[[tert-butyl(dimethyl)silyl]oxy]-12-methyl-1-oxacyclododec-3-en-2-one
RAMARIOLIDE_B
(1R,6S,11aS,13S,14R,14aR)-1,13,14-Trihydroxy-6-methyl-1,6,7,8,9,11a,12,13,14,14a-decahydro-4H-cyclopenta[f]oxacyclotridecin-4-one
(E)-5-[(E)-3-[2,2-dimethyl-5-[2-(2-trimethylsilylethoxymethoxy)propyl]-1,3-dioxolan-4-yl]-1-oxoprop-2-enoxy]-2-hexenoic acid 2-trimethylsilylethyl ester
7-Acetylbrefeldin A
ISOSPOROTHRIC-ACID;(2R)-2-[(1R)-1-HYDROXYHEPTYL]-4-METHYL-5-OXO-2,5-DIHYDRO-FURAN-3-CARBOXYLIC-ACID
(2S,3S,6R,4E)-1-TERT-BUTYLDIMETHYLSILYLOXY-3,6-DI(BENZOYLOXY)-2-HYDROXYHENEICOS-4-ENE
4A,5,6,7,8,8A-HEXAHYDRO-4A-HYDROXY-4-METHYL-2H-1-BENZOPYRAN-2-ON
(4aR,8aS)-4a-hydroxy-4-methyl-6,7,8,8a-tetrahydro-5H-chromen-2-one
| 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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