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2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER

Compound with spectra: 2 NMR

2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER
SpectraBase Compound ID 73TnkiVI54X
InChI InChI=1S/C14H22O2/c1-9-3-4-12-11(8-16-2)10-7-14(9,12)6-5-13(10)15/h9-12H,3-8H2,1-2H3/t9?,10-,11+,12+,14-/m1/s1
InChIKey JGFZTJVOPFQAAY-QBRFGZJISA-N
Mol Weight 222.33 g/mol
Molecular Formula C14H22O2
Exact Mass 222.16198 g/mol
Enantiomer InChIKey JGFZTJVOPFQAAY-KJAYNUCNSA-N

View Spectrum of 2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MINOR-EPIMER
2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.2.1.0(1,5)]-DECAN-8-ONE;MAJOR-EPIMER
6-[[(p-tolylsulfonyl)oxy]methyl]tricyclo[5.3.0.0(2,6)]-3-de-canone
ETHYL-(22-R)-DE-A,B-18,22-CYCLO-8-HYDROXYCHOLAN-24-ATE
3-[(1S,3aS,4S,7aS)-1-[tert-butyl(dimethyl)silyl]oxy-5-keto-7a-methyl-2,3,3a,4,6,7-hexahydro-1H-inden-4-yl]propionic acid methyl ester
(3a.beta.,4.alpha.,6a.alpha.,9a.beta.,10a.alpha.)-Tetradecahydro-4,9a-dimethyl-1-oxodicyclopenta[a,d]cyclooctene-5-carboxylic Acids
93a.beta.,4.beta.,6a.alpha.,9a.beta.,10a.alpha.)-Tetradecahydro-4,9a-dimethyl-1-oxodicyclopenta[a,d]cyclooctene-5-carboxylic Acids
acetic acid [(1S,3R,3aS,4R,5S,6aS)-4-butyl-5-hexyl-6-keto-3-methylol-2,3,3a,4,5,6a-hexahydro-1H-pentalen-1-yl]methyl ester
[4-Hydroxymethyl-2-hexyl-3-butyl-1-oxooctahydropentalen-6-yl]methyl acetate
3,6,6,7b-Tetramethyldecahydro-1H-cyclobuta[e]inden-3-ol
3,3-(Ethylenedioxy)-1,2,6-trimethylbicyclo[4.3.0]nonan-8-one
Title Journal or Book Year
Rearrangements of tricyclic ketones: [3.3.3]propellane formation via a γ-enolate revealed in an approach to the pentalenene skeleton through β-enolization Canadian Journal of Chemistry 1994
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