IVGLLVGUFXDQED-XXFSISAASA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | EptFczHUBeT |
|---|---|
| InChI | InChI=1S/C11H18O2/c1-11-4-7-2-3-10(11)13-6-9(11)8(7)5-12/h7-10,12H,2-6H2,1H3/t7-,8+,9-,10+,11+/m1/s1 |
| InChIKey | IVGLLVGUFXDQED-XXFSISAASA-N |
| Mol Weight | 182.26 g/mol |
| Molecular Formula | C11H18O2 |
| Exact Mass | 182.13068 g/mol |
| Enantiomer InChIKey | IVGLLVGUFXDQED-OGBGREFGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1RS,2RS,3SR,6RS,7SR,10SR)-(3-Methyl-4-oxatricyclo[4.3.1.0(3,7]decan-10-yl)methanol
[1S,3aS,4S,7aS]-(+)-1-tert-Butoxy-4-isopropyl-7a-methyl-3a,4,7,7a-tetrahydro-5(6)-indan-5-one
4-T-Butoxy-12,12-dimethoxy-hexacyclo(5.4.1.0/2,6/.0/3,10/.0/5,9/.0/8,11/)dodecane
2a.beta.,5a.beta.,8,8-Tetramethyl-8a.beta.H,8b.alpha.H-decahydronaptho[1,8-bc]-furan
2a.beta.,5a.beta.,8,8-Tetramethyl-8a.alpha.H,8b.beta.H-decahydronaptho[1,8-bc]-furan
(20R)-de-A,B-8.beta.-(tert-butyldimethylsilyl)oxy-20-(hydroxymethyl)pregnane
8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-DE-A,B-23,24-DINORCHOLAN-22-OL
8,12-epoxy-13,14,15,16,17-pentanorlabdane
13-Ethylenedioxy-14,15-dinor-8-epi-labdan-17-ol
| Title | Journal or Book | Year |
|---|---|---|
| Ether formation by intramolecular attack of hydroxy on cyclopropyl rings: a model for the formation of the tetrahydrofuran moiety in the diterpenoid, harringtonolide | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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