(1R,5S)-2-[(E)-2-[5-[(E)-2-[(1R,5S)-4-keto-7,7-dimethyl-2-bicyclo[3.1.1]hept-2-enyl]vinyl]-2-thienyl]vinyl]-7,7-dimethyl-bicyclo[3.1.1]hept-2-en-4-one
Compound with spectra: 1 NMR
![(1R,5S)-2-[(E)-2-[5-[(E)-2-[(1R,5S)-4-keto-7,7-dimethyl-2-bicyclo[3.1.1]hept-2-enyl]vinyl]-2-thienyl]vinyl]-7,7-dimethyl-bicyclo[3.1.1]hept-2-en-4-one](/api/compound/5fQQUmpuTI7.png?ph=true&h=300&w=458 "(1R,5S)-2-[(E)-2-[5-[(E)-2-[(1R,5S)-4-keto-7,7-dimethyl-2-bicyclo[3.1.1]hept-2-enyl]vinyl]-2-thienyl]vinyl]-7,7-dimethyl-bicyclo[3.1.1]hept-2-en-4-one")
| SpectraBase Compound ID | 5fQQUmpuTI7 |
|---|---|
| InChI | InChI=1S/C26H28O2S/c1-25(2)19-13-21(25)23(27)11-15(19)5-7-17-9-10-18(29-17)8-6-16-12-24(28)22-14-20(16)26(22,3)4/h5-12,19-22H,13-14H2,1-4H3/b7-5+,8-6+/t19-,20-,21+,22+/m0/s1 |
| InChIKey | CAMSEQULRLJNAS-JWENGJAYSA-N |
| Mol Weight | 404.57 g/mol |
| Molecular Formula | C26H28O2S |
| Exact Mass | 404.181001 g/mol |
| Enantiomer InChIKey | CAMSEQULRLJNAS-USSCCXTMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1R,5S)-2-[(E)-2-(2,6-dichlorophenyl)ethenyl]-7,7-dimethylbicyclo[3.1.1]hept-2-en-4-one
Acetic acid 5,5-dimethyl-7-oxo-3,4,4a,5,6,7-hexahydro-naphthalen-2-ylmethyl ester
(4aR,5R)-5-Isopropenyl-8-methyl-4,4a,5,6-tetrahydronaphthalen-2(3H)-one
(4aR,5S)-5-Isopropenyl-8-methyl-4,4a,5,6-tetrahydronaphthalen-2(3H)-one
8-Isopropenyl-5-methyl-1,7,8,8a-tetrahydronaphthalo-4,5-dien-3(2H)-one
Bicyclo[3.1.1]hept-2-ene-3-carboxylic acid, 6,6-dimethyl-4-oxo-, ethyl ester, (1R)-
(+)-(1R,2S,8aR)-1,2,6,7,8,8a-hexahydro-7-hydroxy-1,8a-dimethyl-6-oxonaphthalen-2-yl
1,3-METHANONAPHTHALEN-7(1H)-ONE, 2,3,4,4A,5,6-HEXAHYDRO-2,2-DIMETHYL-
Drima-7,9(11)-diene
5-(2',6'-Dimethylbicyclo[3.1.1]hept-2'-en-6'-yl)-2-methylpentane-2,3,4-triol
| Title | Journal or Book | Year |
|---|---|---|
| Novel Reactivity of SeO2 with 1,3-Dienes: Selenophene Formation | The Journal of Organic Chemistry | 2002 |