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(+/-)-MESEMBRANONE

Compound with spectra: 3 NMR, and 1 MS (GC)

(+/-)-MESEMBRANONE
SpectraBase Compound ID 3CgHgET8Prp
InChI InChI=1S/C17H23NO3/c1-18-9-8-17(7-6-13(19)11-16(17)18)12-4-5-14(20-2)15(10-12)21-3/h4-5,10,16H,6-9,11H2,1-3H3/t16-,17-/m0/s1
InChIKey DAHIQPJTGIHDGO-IRXDYDNUSA-N
Mol Weight 289.38 g/mol
Molecular Formula C17H23NO3
Exact Mass 289.167794 g/mol
Enantiomer InChIKey DAHIQPJTGIHDGO-IAGOWNOFSA-N

View Spectrum of (+/-)-MESEMBRANONE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum RCM-35-SM3-7

View Spectrum of (+/-)-MESEMBRANONE

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

View Spectrum of (+/-)-MESEMBRANONE

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

View Spectrum of (+/-)-MESEMBRANONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (+/-)-MESEMBRINE
  • Mesembrine
Mesembrin
Mesembrine
(-)-Mesembranol
1H-Indol-6-ol, octahydro-3a-(4-hydroxy-3-methoxyphenyl)-1-methyl-, [3aS-(3a.alpha.,6.beta.,7a.alpha.)]-
1-((1S,2S)-2-azido-1-(3,4-dimethoxyphenyl)cyclohexyl)ethanone
Benzenesulfonic acid, 2-[2-[[4-cyano-4-(3,4-dimethoxyphenyl)-5-methylhexyl]methylamino]ethyl]-4,5-dimethoxy-
Benzenesulfonic acid, 2-[2-[[4-cyano-4-(3,4-dimethoxyphenyl)-5-methylhexyl]methylamino]ethyl]-4,5-dimethoxy-, sodium salt
3-(1,3-Benzodioxol-5-yl)-4-(2-methoxycarbonylethyl)-N-methyl-4-nitropyrrolidine
benzeneacetamide, N-[2-(3,4-dimethoxyphenyl)ethyl]-N-[2,5-dioxo-1-(4-propoxyphenyl)-3-pyrrolidinyl]-
Ethyl (2R,3R,4S)-2-(4-methoxyphenyl)-4-(3,4-(metrhylenedioxy)phenyl)pyrrolidine-3-carboxylate
Methyl (3a.alpha.,7.beta.,7a.alpha.)-7-(1',3'-benzodioxol-5'-yl)octahydro-1H-indole-1-carboylate
9,10-dimethoxy-1,6,7,11b-tetrahydrobenzo[a]quinolizin-2-one
Title Journal or Book Year
Influencing the Balance between ipso and ω Nucleophile Addition to (1-Arylcyclohexadienyl)iron Intermediates in Alkaloid Synthesis European Journal of Organic Chemistry 2012
On the Synthesis of (±)-Mesembranone by the Dissolving Metal Reduction of 4-Aryl-4-aminoethylcyclohexenones. Isolation of N-Methyl-5-(3',4'-dimethoxyphenyl)-2-azabiocyclo[3.3.1]nonan-8-one HETEROCYCLES 1985
Carbon-13 Nuclear Magnetic Resonance in Alkaloid Chemistry HETEROCYCLES 1983
Mesembrine
Mesembrin
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