METHYL-(1R,3R,3AR,6R,8S)-3-ACETOXY-8-HYDROXY-5-OXO-1,2,3,4,5,6-HEXAHYDRO-3A,6-ETHANO-3AH-INDENE-1-CARBOXYLATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 3r0QeArFpcw |
|---|---|
| InChI | InChI=1S/C15H18O6/c1-7(16)21-13-4-8(14(19)20-2)10-3-9-11(17)5-15(10,13)6-12(9)18/h3,8-9,11,13,17H,4-6H2,1-2H3/t8-,9-,11+,13-,15-/m1/s1 |
| InChIKey | QLUZYMRJXMXDEH-VXOUJVJRSA-N |
| Mol Weight | 294.3 g/mol |
| Molecular Formula | C15H18O6 |
| Exact Mass | 294.110338 g/mol |
| Enantiomer InChIKey | QLUZYMRJXMXDEH-CEBDARMXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
8-SYN-METHYL-(1R,3R,3AR,6R,8S)-3-DICHLOROACETOXY-8-HYDROXY-5-OXO-1,2,3,4,5,6-HEXAHYDRO-3A,6-ETHANO-3AH-INDENE-1-CARBOXYLATE
Methyl (1R*,3R*,3aR*,6R*,8R*)-3-acetoxy-8-hydroxy-5-oxo-1,2,3,4,5,6-hexahydro-3a,6-ethano-3aH-indene-1-carboxylate
Androst-7-en-3-one, 17-(acetyloxy)-19-hydroxy-4,4-dimethyl-, (5.alpha.,13.alpha.,17.beta.)-
CONFERTIFOLINE,6-B-ACETOXY-7-A-CHLORO
No Name
(1R,2R,3S,4S,5S,6S)-IODOLACTONE
ENT-16-beta-HYDROXY-11-KAUREN-19-OIC ACID
1-ALPHA-HYDROXY-4-BETA-ACETOXYPSEUDOGUAIAN-6-BETA,12-OLIDE;AMBrOSANOLIDE
3-BETA,19-DIHYDROXY-8-(9),15-ISOPIMARADIEN-7-ONE
2aR*,3R*,8bS*-2a,8b-dihydroxy-7-methoxy-3-(p-methoxyphenyl)-1,2,3,4-tetrahydrocyclobut[c]quinoline
| Title | Journal or Book | Year |
|---|---|---|
| An Approach to the Total Synthesis of Diterpenoid Plant Growth Substances Isolated From Gametophytes of the Fern Genus Anemia | Australian Journal of Chemistry | 1992 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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