20,22-EPOXY-2,10,19,21-CLADOCORATETRAEN-18-ONE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | D8q6DXj77PK |
|---|---|
| InChI | InChI=1S/C25H36O2/c1-18(2)8-6-13-24(4)14-7-9-22-21(24)11-10-19(3)25(22,5)16-23(26)20-12-15-27-17-20/h9,12,15,17,19,21H,1,6-8,10-11,13-14,16H2,2-5H3/t19-,21+,24+,25+/m1/s1 |
| InChIKey | NJRQRHDVDCADNN-BDBQITIBSA-N |
| Mol Weight | 368.6 g/mol |
| Molecular Formula | C25H36O2 |
| Exact Mass | 368.27153 g/mol |
| Enantiomer InChIKey | NJRQRHDVDCADNN-KOSPYUSVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
20,22-EPOXY-2,10,19,21-CLADOCORATETRAEN-18S-OL
20,22-EPOXY-2,10,19,21-CLADOCORATETRAEN-18R-OL
ETHYL-15-METHOXY-18A-HOMO-1(10),13E-ENT-HALIMADIEN-18-OATE
Methyl 15-tetrahydropyranyloxy-ent-halima-1(10),13E-dien-18-xantogenate
15-METHOXY-1(10),13E-ENT-HALIMADIEN-18-YL-CHLORIDE
ACETOXYHYDROHALIMIC-ACID
HYDROHALIMIC-ACID
METHYL-13,14,15,16-TETRANOR-12-HYDROXY-1(10)-ENT-HALIMEN-18-OATE
Methyl 12-Hydroxy-13,14,15,16-tetranor-ent-halima-1(10)-en-18-oate
Methyl 12-Oxo-13,14,15,16-tetranor-ent-halima-1(10)-en-18-oate
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Bioactive Sesterterpenolides from ent-Halimic Acid. 15-Epi-ent-cladocoran A and B | The Journal of Organic Chemistry | 2003 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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