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(+)-CORONARINE

Compound with spectra: 3 NMR, and 3 MS (GC)

(+)-CORONARINE
SpectraBase Compound ID 70oC2rWR7qC
InChI InChI=1S/C20H28O/c1-15-6-9-18-19(2,3)11-5-12-20(18,4)17(15)8-7-16-10-13-21-14-16/h7-8,10,13-14,17-18H,1,5-6,9,11-12H2,2-4H3/b8-7+/t17-,18-,20+/m0/s1
InChIKey QXVXYNOIXUIXBI-NDLVVHCESA-N
Mol Weight 284.44 g/mol
Molecular Formula C20H28O
Exact Mass 284.214016 g/mol
Enantiomer InChIKey QXVXYNOIXUIXBI-HOZMWOPPSA-N

View Spectrum of (+)-CORONARINE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-44-1793-2

View Spectrum of (+)-CORONARINE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-66-1626-1

View Spectrum of (+)-CORONARINE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-60-907-3

View Spectrum of (+)-CORONARINE

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

View Spectrum of (+)-CORONARINE

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

View Spectrum of (+)-CORONARINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Coronarin E
  • 3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]furan
Coronarin E
Coronarin A
15-HYDROXY-LABDA-8(17),11,13-TRIEN-16-AL-[E,E]
(E,E)-15-Hydroxy-Labda-8(17),11,13-trien-16-al
CALCARATARIN-A;(E)-LABDA-8(17),12-DIEN-15,15-DIMETHOXY-16-AL
AFRAMOLIN_A;15-HYDROXY-15-METHOXYLABDA-8-(17),12-(E)-DIEN-16-AL
LABDA-8(17),13E-DIEN-15-YL-BENZOATE
LABDA-8(17),13Z-DIEN-15-YL-BENZOATE
LABDA-8(17),13E-DIEN-15-YL-PARA-NITROBENZOATE
LABDA-8(17),13Z-DIEN-15-YL-PARA-NITROBENZOATE
(12-Z,14-R)-LABDA-8-(17),12-DIENE-14,15,16-TRIOL
1-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]pent-3-yn-2-one
Title Journal or Book Year
Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol Journal of Natural Products 2003
A Concise Conversion of (−)-Sclareol into (+)-Coronarin E and (−)-7-epi-Coronarin A Journal of Natural Products 1998
Labdane Diterpenoids from Alpinia chinensis Journal of Natural Products 1997
Coronarin E
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