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RAC-(1R,4S,4AR,9BS)-6-ACETYL-7,9-DIMETHOXY-1-(1-METHYLETHYL)-1,2,3,4,4A,9B-HEXAHYDRODIBENZOFURAN-4-SPIRO-4'-DIOXORAN-2'-ONE

Compound with spectra: 1 NMR

RAC-(1R,4S,4AR,9BS)-6-ACETYL-7,9-DIMETHOXY-1-(1-METHYLETHYL)-1,2,3,4,4A,9B-HEXAHYDRODIBENZOFURAN-4-SPIRO-4'-DIOXORAN-2'-ONE
SpectraBase Compound ID 62xqH9tBR4I
InChI InChI=1S/C21H26O7/c1-10(2)12-6-7-21(9-26-20(23)28-21)19-16(12)17-14(25-5)8-13(24-4)15(11(3)22)18(17)27-19/h8,10,12,16,19H,6-7,9H2,1-5H3/t12-,16+,19-,21+/m1/s1
InChIKey GWFDKEODXYBEON-KDBGMYCZSA-N
Mol Weight 390.43 g/mol
Molecular Formula C21H26O7
Exact Mass 390.167853 g/mol
Enantiomer InChIKey GWFDKEODXYBEON-HTQCQZDPSA-N

View Spectrum of RAC-(1R,4S,4AR,9BS)-6-ACETYL-7,9-DIMETHOXY-1-(1-METHYLETHYL)-1,2,3,4,4A,9B-HEXAHYDRODIBENZOFURAN-4-SPIRO-4'-DIOXORAN-2'-ONE

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
First Total Synthesis of (±)-Linderol A, a Tricyclic Hexahydrodibenzofuran Constituent of Lindera umbellata Bark, with Potent Inhibitory Activity on Melanin Biosynthesis of Cultured B-16 Melanoma Cells The Journal of Organic Chemistry 2003

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