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2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.2.1.0(1,5)]-DECAN-8-ONE;MAJOR-EPIMER

Compound with spectra: 2 NMR

2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.2.1.0(1,5)]-DECAN-8-ONE;MAJOR-EPIMER
SpectraBase Compound ID 5mLiEAyGe8Z
InChI InChI=1S/C13H20O2/c1-8-3-4-11-10(7-15-2)9-5-13(8,11)6-12(9)14/h8-11H,3-7H2,1-2H3/t8?,9-,10+,11+,13+/m1/s1
InChIKey ADCSTPYNEMVSHV-BJBJFPRCSA-N
Mol Weight 208.3 g/mol
Molecular Formula C13H20O2
Exact Mass 208.14633 g/mol
Enantiomer InChIKey ADCSTPYNEMVSHV-XQRRBWBPSA-N

View Spectrum of 2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.2.1.0(1,5)]-DECAN-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-[5.2.1.0(1,5)]-DECAN-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-[5.2.1.0(1,5)]-DECAN-8-ONE;MINOR-EPIMER
2-METHYL-EXO-6-METHOXYMETHYL-TRICYCLO-[5.3.1.0(1,5)]-UNDECAN-8-ONE;MAJOR-EPIMER
2',6-dimethyl-5'-propan-2-yl-5-spiro[7-oxabicyclo[4.1.0]heptane-3,1'-cyclopentane]one
[6-Hydroxymethyl-2-propyl-3-butyl-1-oxooctahydropentalen-4-yl]methyl acetate
(2R,4aR,5R,8R,8aS)-2,5-dimethyl-4a-oxidanyl-8-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-one
(1a.alpha.,1b.beta.,5a.alpha.,6a.alpha.)-octahydro-1b-methylspiro[cycloprop[a]indene-4(1H),2'-[1,3]dioxolan]-6-one
(2R,3R)-diethyl 4,4-dimethyl-2-pentyl-3-(phenylthiomethyl)cyclopentane-1,1-dicarboxylate
5-ALPHA,10-ALPHA,11-TRIHYDROXYAMORPHAN-3-ONE
(4S)-10-ALPHA,15-EPOXY-12-HYDROXYCADINAN-3-ONE
Spiro[4.5]dec-7-ene-1-butanoic acid, 9-hydroxy-8-(methoxycarbonyl)-.gamma.,4-dimethyl-, 1-methylethyl ester, [1R-[1.alpha.(R*),4.beta.,5.beta.(S*)]]-
1,1,3,3(2H,3aH)-Pentalenetetracarboxylic acid, tetrahydro-5,5-dimethoxy-, tetramethyl ester
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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