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15,16-EPOXY-12-HYDROXY-LABDA-8(17),13(16),14-TRIENE

Compound with spectra: 1 NMR, and 2 MS (GC)

15,16-EPOXY-12-HYDROXY-LABDA-8(17),13(16),14-TRIENE
SpectraBase Compound ID 5Df1DkzqYrh
InChI InChI=1S/C20H30O2/c1-14-6-7-18-19(2,3)9-5-10-20(18,4)16(14)12-17(21)15-8-11-22-13-15/h8,11,13,16-18,21H,1,5-7,9-10,12H2,2-4H3/t16-,17?,18-,20+/m0/s1
InChIKey HJODEDKXJPYIBN-FXCQJFQISA-N
Mol Weight 302.46 g/mol
Molecular Formula C20H30O2
Exact Mass 302.22458 g/mol
Enantiomer InChIKey HJODEDKXJPYIBN-FLANGGGJSA-N

View Spectrum of 15,16-EPOXY-12-HYDROXY-LABDA-8(17),13(16),14-TRIENE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-66-1626-9a

View Spectrum of 15,16-EPOXY-12-HYDROXY-LABDA-8(17),13(16),14-TRIENE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-66-1626-9b

View Spectrum of 15,16-EPOXY-12-HYDROXY-LABDA-8(17),13(16),14-TRIENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decalin-1-yl]-1-(3-furyl)ethanol
FURANOLABDANE-ALCOHOL
FURANOLABDANE-ALCOHOL
(1S / 1R)-2-Methylene-5,5,9-trimethyl-1-[2'-(3''-furyl)-2''-hydroxyethyl]-(perhydro)-naphthalene
(1R / 1S)-2-Methylene-5,5,9-trimethyl-1-[2'-(3''-furyl)-2''-hydroxyethyl]-(perhydro)-naphthalene
12-XI,15-DIHYDROXY-LABDA-8(17)-13-DIEN-16-AL-[E]
12.eta.,15-Dihydroxy-Labda-8(17),13-dien-16-al
2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-furan-3-ylethanone
(E)-3-Methyl-5-((1R,8aR)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl)-pent-2-enoic acid (R)-2-acetoxy-3-(tert-butyl-dimethyl-silanyloxy)-propyl ester
Isocoronarin-D
14-BETA-HYDROXY-LABDA-8(17),12-DIEN-15(16)-OLIDE
CALCARATARIN-D;14-EPI-ISOCORONARIN-D;LABDA-8(17),12-DIEN-14-ALPHA-OL-16(15)-OLIDE
2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-(4-methoxyphenyl)ethanone
Title Journal or Book Year
A Concise Conversion of (−)-Sclareol into (+)-Coronarin E and (−)-7-epi-Coronarin A Journal of Natural Products 1998

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