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12,19-DIHYDROXY-13,14,15,16-TETRANORLABD-8(17)-ENE

Compound with spectra: 2 NMR

12,19-DIHYDROXY-13,14,15,16-TETRANORLABD-8(17)-ENE
SpectraBase Compound ID A1eVIi8YWz9
InChI InChI=1S/C16H28O2/c1-12-5-6-14-15(2,11-18)8-4-9-16(14,3)13(12)7-10-17/h13-14,17-18H,1,4-11H2,2-3H3/t13-,14?,15+,16+/m0/s1
InChIKey VOHQEKLLPZAHLR-QWICORGASA-N
Mol Weight 252.4 g/mol
Molecular Formula C16H28O2
Exact Mass 252.20893 g/mol
Enantiomer InChIKey VOHQEKLLPZAHLR-PLZVMKCUSA-N

View Spectrum of 12,19-DIHYDROXY-13,14,15,16-TETRANORLABD-8(17)-ENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of 12,19-DIHYDROXY-13,14,15,16-TETRANORLABD-8(17)-ENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • 13,14,15,16-TETRANORLABD-8(17)-ENE-12,19-DIOL
1-Naphthaleneethanol, decahydro-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-, [1S-(1.alpha.,4a.beta.,5.alpha.,8a.alpha.)]-
RIYUSAKJWZXQID-ZQDZILKHSA-N
8(12),17-SACCULATADIEN-11-OL
14,15-DEHYDROMANOOL
(14RS)-LABD-8(17)-ENE-13,14-DIOL
GDLNVLRBWGTNDA-HYBGUHBYSA-N
16-ACETOXY-ENT-LABDA-8(17),13Z-DIEN-15-OIC-ACID-METHYLESTER
LABDA-8(17),13E-DIEN-15-YL-BENZOATE
LABDA-8(17),13Z-DIEN-15-YL-BENZOATE
Verrucosin-5
Title Journal or Book Year
Microbial hydroxylation/functionalization of terpenoid synthons derived from communic acids Phytochemistry 2000
Chemistry of the Podocarpaceae. LXXIV. The Conversion of Podocarpic Acid Into γ-Bicyclohomofarnesals Australian Journal of Chemistry 1989

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