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Ethyl rac-(1R,3aR,8bS)-3-Hydroxy-6,8-dimethoxy-1-(1-methylethyl)-3a,8b-dihydro-1H-cyclopenta[b]benzofuran-2-carboxylate

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

Ethyl rac-(1R,3aR,8bS)-3-Hydroxy-6,8-dimethoxy-1-(1-methylethyl)-3a,8b-dihydro-1H-cyclopenta[b]benzofuran-2-carboxylate
SpectraBase Compound ID LDnFUdZZjII
InChI InChI=1S/C19H24O6/c1-6-24-19(21)16-13(9(2)3)15-14-11(23-5)7-10(22-4)8-12(14)25-18(15)17(16)20/h7-9,13,15,18,20H,6H2,1-5H3/t13-,15+,18-/m1/s1
InChIKey IJECGMWUZJBIIT-QIIPPGSGSA-N
Mol Weight 348.4 g/mol
Molecular Formula C19H24O6
Exact Mass 348.157288 g/mol
Enantiomer InChIKey IJECGMWUZJBIIT-JOQOYGCGSA-N

View Spectrum of Ethyl rac-(1R,3aR,8bS)-3-Hydroxy-6,8-dimethoxy-1-(1-methylethyl)-3a,8b-dihydro-1H-cyclopenta[b]benzofuran-2-carboxylate

MS (GC) Spectrum
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Source of Spectrum F-68-1221-6

View Spectrum of Ethyl rac-(1R,3aR,8bS)-3-Hydroxy-6,8-dimethoxy-1-(1-methylethyl)-3a,8b-dihydro-1H-cyclopenta[b]benzofuran-2-carboxylate

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
exo-Benzyl rel(1R,4aR,9bS)-1,2,4a,9b-tetrahydro-4-hydroxy-7,9-dimethoxy-1-(1-methylethyl)-3-dibenzofurancarboxylate
[(Trimethylsilyl)ethyl] (1R,4aR,9bS)-1,2,4a,9b-tetrahydro-4-hydroxy-1-(1'-methylethyl)-7,9-dimethoxy-dibenzofuran-3-carboxylate
tert-Butyl rel-(1R,4aR,9bS)-1,2,4a,9b-tetrahydro-4-hydroxy-7,9-dimethoxy-1-(1-methylethyl)-3-dibenzofurancarboxylate
3,9-bis(benzyloxy)-6,6-dimethyl-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-ol
[(8-([Dimethyl(phenyl)silyl]oxy)-6,6,9-trimethyl-3-pentyl-6a,7,8,10a-tetrahydro-6H-benzo[c]chromen-1-yl)oxy](dimethyl)phenylsilane
3β-hydroxyandrost-5-eno[17,16-b]furan-5'-one
O,2-PROPANO-DELTA(8)-TETRAHYDROCANNABINOL
1H-Furo[3,4-a]carbazole-1,3(10H)-dione, 10-(phenylmethyl)-
2-Isopropyl-4a,7-epoxy-8-methylene-4,4-dimethoxy-1,2,3,4,7,4a,8a-octahydronaphth-1-ol
SCHWEINFURTHIN_H
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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