(E)-2-ACETOXY-7-HYDROXY-ADAMANTANE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | AOkRgnhCEDS |
|---|---|
| InChI | InChI=1S/C12H18O3/c1-7(13)15-11-9-2-8-3-10(11)6-12(14,4-8)5-9/h8-11,14H,2-6H2,1H3/t8-,9-,10-,11-,12-/m0/s1 |
| InChIKey | LUFGSGKNQLDQDE-HTFCKZLJSA-N |
| Mol Weight | 210.27 g/mol |
| Molecular Formula | C12H18O3 |
| Exact Mass | 210.125594 g/mol |
| Enantiomer InChIKey | LUFGSGKNQLDQDE-LZQZFOIKSA-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 |
- (Z)-2-ACETOXY-5-HYDROXY-ADAMANTANE
(Z)-2-ACETOXY-5-FLUOROADAMANTANE
(Z)-2-METHOXY-5-TERT.-BUTYLADAMANTANE
(E)-2-METHOXY-5-TERT.-BUTYLADAMANTANE
SYN-2-HYDROXY-5-ACETOXYADAMANTANE
(E)-5-DEUTERO-2-TRIMETHYLSILYLOXYADAMANTANE
(Z)-5-DEUTERO-2-TRIMETHYLSILYLOXYADAMANTANE
(E)-5-Chloro-2-trimethylsilyloxy-adamantane
5-trimethylsilyladamantan-2-ol
5-(trimethylstannyl)adamatan-2-ol
(Z)-5-BROMOADAMANTANE-2-CARBOXYLIC_ACID
| Title | Journal or Book | Year |
|---|---|---|
| Hyperconjugative Control by Remote Substituents of Diastereoselectivity in the Oxygenation of Hydrocarbons | Organic Letters | 2000 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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