SASUSSUREA-LACTONE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | HEYOMem3hYC |
|---|---|
| InChI | InChI=1S/C15H22O2/c1-6-15(5)8-7-11-10(4)14(16)17-13(11)12(15)9(2)3/h6,10-13H,1-2,7-8H2,3-5H3/t10-,11-,12+,13-,15+/m0/s1 |
| InChIKey | LMNJALUUIMXUQQ-DKBOKBLXSA-N |
| Mol Weight | 234.34 g/mol |
| Molecular Formula | C15H22O2 |
| Exact Mass | 234.16198 g/mol |
| Enantiomer InChIKey | LMNJALUUIMXUQQ-VVSAWPALSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 5,7-ALPHA-H,6,11-BETA-H-ELEMA-1,3-DIEN-6,12-OLIDE
2(3H)-Benzofuranone, 6-ethenylhexahydro-6-methyl-3-methylene-7-(1-methylethenyl)-, [3aS-(3a.alpha.,6.alpha.,7.beta.,7a.beta.)]-
PQQBWZPCMSAPQA-PWRIRTTLSA-N
(1R,2R,3S,4R)-3-[(4'-Hydroxy-4'-methyl-1'-oxopent-2'-enyl)oxy]-2-isopropenyl-1-vinyl-1-methyl-4-acetylcyclohexane
1-OXO-5-ALPHA,6-BETA,7-ALPHA-H-2-NORELEMA-3,11(13)-DIEN-12,6-OLIDE
4-B-H,5-A-H,11-B-H-EUDESMAN-12,6-A-OLIDE,3-A-HYDROXY
4-beta-H,5-alpha-H,11-beta-H-EUDESMAN-12,6-alpha-OLIDE,3-beta-HYDROXY
4-A-H,5-B-H,11-B-H-EUDESMAN-12,6-A-OLIDE,3-A-HYDROXY
3a-Hydroxy-5,7aH,4,6,11bH-eudesman-6,12-olide
3.alpha.-Hydroxy-4.alpha.,5.alpha.11.beta.-H-eudesman-6.alpha.,12-olide
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of (+)-8-Deoxyvernolepin and Its 11,13-Dihydroderivative. A Novel Reaction Initiated by Sulfene Elimination Leads to the 2-Oxa-cis-decalin Skeleton | The Journal of Organic Chemistry | 2002 |
| Synthesis of torrentin, dihydrosantamarine, and saussurea lactone from santonin | Canadian Journal of Chemistry | 1992 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.