2-DESOXY-11-BETA,13-DIHYDRO-EPIPARTHEMOLLIN
Compound with spectra: 2 NMR
| SpectraBase Compound ID | 6LWSiSBk8jN |
|---|---|
| InChI | InChI=1S/C15H22O3/c1-9-4-7-13-11(3)15(17)18-14(13)8-12(9)6-5-10(2)16/h8-9,11,13-14H,4-7H2,1-3H3/t9-,11-,13-,14+/m0/s1 |
| InChIKey | YMEVSAAYOZFKIF-DTCNJJKHSA-N |
| Mol Weight | 250.34 g/mol |
| Molecular Formula | C15H22O3 |
| Exact Mass | 250.156895 g/mol |
| Enantiomer InChIKey | YMEVSAAYOZFKIF-IMJCEVDSSA-N |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Solvent | Chloroform |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- PARTHEMOLLIN,6-EPI,2-DESOXY-11-B,13-DIHYDRO
LACTULIDE A
SHONACALIN S
11-B-H-GERMACRA-1(10)E,4E-DIEN-12,6-A-OLIDE,3-B,14-DIHYDROXY
SHONACHALIN C
GSLRFQSAMMVDEI-YDHNIYMWSA-N
HERBOLIDE A,DESACETYL
BALCHANOLIDE
1-ALPHA,8-ALPHA-DIHYDROXY-GERMACRA-4E,9Z-DIEN-6-BETA,7-ALPHA-11-BETA-H-12,6-OLIDE
(2e,6e,10e)-1-(2.alpha.-isopropyl-5.beta.-methylcyclohexoxyacetyloxy)-14-isopropenyl-3,7,11-trimethylcyclotetradecatriene
| Title | Journal or Book | Year |
|---|---|---|
| Biomimetic Transformations of 11,13-Dihydroparthenolide and Oxidative Rearrangements ofa Guai- 1(10)-en-6,12-olide | Journal of Natural Products | 1989 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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