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

Compound with spectra: 1 NMR

(5S)-6-OXA-5-METHYL-1,2,3-TRIMETHOXY-9,12A-EPOXY-5,7,9,11,12,12A-HEXAHYDROBENZO-[A]-HEPTALENE-10-OL
SpectraBase Compound ID DFM7cTf95K1
InChI InChI=1S/C19H24O6/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/h7-8,10,13-14,20H,5-6,9H2,1-4H3/t10-,13-,14+,19+/m1/s1
InChIKey XBRJOQFAIGMBLB-OOOLOXNWSA-N
Mol Weight 348.4 g/mol
Molecular Formula C19H24O6
Exact Mass 348.157288 g/mol
Enantiomer InChIKey XBRJOQFAIGMBLB-KNBXBXJZSA-N

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

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