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(1-BETA,7-BETA,11-BETA)-8-ALPHA-DIMETHOXYMETHYL-8-BETA-METHYL-3-AZA-2-OXYTRICYCLO-[5.3.1.0(4,11)]-UNDEC-3-ENE

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

(1-BETA,7-BETA,11-BETA)-8-ALPHA-DIMETHOXYMETHYL-8-BETA-METHYL-3-AZA-2-OXYTRICYCLO-[5.3.1.0(4,11)]-UNDEC-3-ENE
SpectraBase Compound ID KfKJaOtFt97
InChI InChI=1S/C13H21NO3/c1-13(12(15-2)16-3)7-6-10-11-8(13)4-5-9(11)14-17-10/h8,10-12H,4-7H2,1-3H3/t8-,10-,11-,13+/m0/s1
InChIKey BEIANNRJLPESJS-KYVBTAMFSA-N
Mol Weight 239.31 g/mol
Molecular Formula C13H21NO3
Exact Mass 239.152144 g/mol
Enantiomer InChIKey BEIANNRJLPESJS-VUXODMRMSA-N

View Spectrum of (1-BETA,7-BETA,11-BETA)-8-ALPHA-DIMETHOXYMETHYL-8-BETA-METHYL-3-AZA-2-OXYTRICYCLO-[5.3.1.0(4,11)]-UNDEC-3-ENE

MS (GC) Spectrum
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Source of Spectrum KC-0-3477-25

View Spectrum of (1-BETA,7-BETA,11-BETA)-8-ALPHA-DIMETHOXYMETHYL-8-BETA-METHYL-3-AZA-2-OXYTRICYCLO-[5.3.1.0(4,11)]-UNDEC-3-ENE

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1.beta.,7.beta.,11.beta.)-8.alpha.-Dimethoxymethyl-8.beta.-methyl-3-aza-2-oxatricyclo[5.3.1.0(4,11)]undec-3-ene
  • (R)-5-Dimethoxymethyl-5-methyl-3,4,4a,5,6,7,7a,7b-octahydro-indeno[1,7-cd]isoxazole
10-ALPHA,14H-1-EPI-INUVISCOLIDE
3-Hydroxy-9-.beta.-acetoxy-11(12)-en-7-.alpha.H-eudesmane
SBBLNZHMSNQOSO-XCUOPRSFSA-N
7-Oxabicyclo[2.2.1]heptane-2,3-dimethanol, 1-(dimethoxymethyl)-, dimethanesulfonate, (exo,exo)-(.+-.)-
1,2-Benzisoxazole-3-carboxylic acid, 3a,4,5,6,7,7a-hexahydro-7a-phenyl-, ethyl ester
3-[(3'aS,4'S,7'aS)-1'-keto-7'a-methyl-spiro[1,3-dioxolane-2,5'-2,3,3a,4,6,7-hexahydroindene]-4'-yl]propionic acid methyl ester
2,6-Ethano[1]benzothieno[5,6-b]oxirene, octahydro-, 3,3-dioxide
Rac-(3aR,4R,7S,7aR,8S)-8-Methoxy-4-methylhexahydro-4,7-methanobenzofuran-2(3H)-one
(1.alpha.)-2.alpha.-Methyl-2.beta.-(1.beta.-methyl-2.alpha.-methylsulfonyloxymethylcyclopenty)cyclohexyl benzoate
(1.beta.)-2.alpha.-Methyl-2.beta.-(1.beta.-methyl-2.alpha.-methylsulfonyloxymethylcyclopenty)cyclohexyl benzoate
Title Journal or Book Year
Synthesis of the A/E/F sections of conaconitine, napelline and related diterpenoid alkaloids of the aconitine group Journal of the Chemical Society, Perkin Transactions 1 1998
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