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(5R,9S,12AS)-6-OXA-5-METHYL-1,2,3-TRIMETHOXY-9,12A-EPOXY-5,7,9,11,12,12A-HEXAHYDROBENZO-[A]-HEPTALENE-10-ONE

Compound with spectra: 2 NMR

(5R,9S,12AS)-6-OXA-5-METHYL-1,2,3-TRIMETHOXY-9,12A-EPOXY-5,7,9,11,12,12A-HEXAHYDROBENZO-[A]-HEPTALENE-10-ONE
SpectraBase Compound ID LPnRLf0LuvW
InChI InChI=1S/C19H22O6/c1-10-12-8-15(21-2)17(22-3)18(23-4)16(12)19-6-5-13(20)14(25-19)7-11(19)9-24-10/h7-8,10,14H,5-6,9H2,1-4H3/t10-,14+,19+/m1/s1
InChIKey XTZSFIXVQWTDEP-UOTLPGLASA-N
Mol Weight 346.38 g/mol
Molecular Formula C19H22O6
Exact Mass 346.141638 g/mol
Enantiomer InChIKey XTZSFIXVQWTDEP-PJZBOPKMSA-N

View Spectrum of (5R,9S,12AS)-6-OXA-5-METHYL-1,2,3-TRIMETHOXY-9,12A-EPOXY-5,7,9,11,12,12A-HEXAHYDROBENZO-[A]-HEPTALENE-10-ONE

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

View Spectrum of (5R,9S,12AS)-6-OXA-5-METHYL-1,2,3-TRIMETHOXY-9,12A-EPOXY-5,7,9,11,12,12A-HEXAHYDROBENZO-[A]-HEPTALENE-10-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (RAC)-(5R,9S,12AS)-6-OXA-5-METHYL-1,2,3-TRIMETHOXY-9,12A-EPOXY-5,7,9,11,12,12A-HEXAHYDROBENZO-[A]-HEPTALEN-10-ONE
Title Journal or Book Year
Synthesis of Oxa-B-Ring Analogs of Colchicine through Rh-Catalyzed Intramolecular [5+2] Cycloaddition European Journal of Organic Chemistry 2012
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