7-BETA,14-DYHYDROXYAROMADENDRANE
Compound with spectra: 3 NMR
| SpectraBase Compound ID | 406pIpxkxuN |
|---|---|
| InChI | InChI=1S/C15H26O2/c1-9-4-5-10-12(9)13-11(14(13,2)8-16)6-7-15(10,3)17/h9-13,16-17H,4-8H2,1-3H3/t9-,10-,11-,12-,13-,14+,15-/m1/s1 |
| InChIKey | PEYLVIRXSYMEHY-LPZKKVOTSA-N |
| Mol Weight | 238.37 g/mol |
| Molecular Formula | C15H26O2 |
| Exact Mass | 238.19328 g/mol |
| Enantiomer InChIKey | PEYLVIRXSYMEHY-YQFOFLOKSA-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 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- (-)-13-HYDROXYGLOBULOL
- 14-EXOHYDROXYGLOBULOL ; (1S,2S,3S,4R,7R,8R,11R)-3-HYDROXYMETHYL-3,7,11-TRIMETHYLTRICYCLO(6.3.0.02,4)UNDECAN-7-OL
Fluorensadiol
Flourensadiol
14-ENDOHYDROXYGLOBULOL ; (1S,2S,3R,4R,7R,8R,11R)-3-HYDROXYMETHYL-3,7,11-TRIMETHYLTRICYCLO(6.3.0.02,4)UNDECAN-7-OL
14-ENDOHYDROXYGLOBULOL ; (1S,2S,3R,4R,7R,8R,11R)-3-HYDROXYMETHYL-3,7,11-TRIMETHYLTRICYCLO(6.3.0.02,4)UNDECAN-7-OL
7-ALPHA,14-DYHYDROXYAROMADENDRANE
14-EXOHYDROXYGLOBULOL ; (1S,2S,3S,4R,7R,8R,11R)-3-HYDROXYMETHYL-3,7,11-TRIMETHYLTRICYCLO(6.3.0.02,4)UNDECAN-7-OL
(-)-10(R)-ISOTHIOCYANO-ALLOAROMADENDRANE
(-)-10(S)-ISOTHIOCYANO-ALLOAROMADENDRANE
(1R,2R,5S,6R,7R,8S)-2,8-Dimethyl-2-thioisocyanato-5,6-isopropylidenebicyclo[5.3.0]decane
(-)-10(R)-ISOTHIOCYANO-AROMADENDRANE
3-OXO-10-ALLOAROMADENDRANOL
3-Oxo-10,14H-alloaromadendran
3.beta.,10.alpha.-Dihydroxy-1,5.alpha.H.4,6,7.beta.H-armadendrane
4.beta.,10.alpha.-Aromadendranediol
(+)-Alloaromadendrane-7.alpha.,11.beta.-diol
| Title | Journal or Book | Year |
|---|---|---|
| Biotransformation of sesquiterpenoids, (−)-globulol and (+)-ledol by Glomerella cingulata | Phytochemistry | 1994 |
| The hydroxylation of globulol and 7-epiglobulol by Cephalosporium aphidicola | Phytochemistry | 1994 |
| Microbial oxidation of tricyclic sesquiterpenoids containing a dimethylcyclopropane ring | Phytochemistry | 1992 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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