Collect. Czech. Chem. Commun.
1987, 52, 1786-1802
https://doi.org/10.1135/cccc19871786
Configuration of natural 9-hydroxyfuroeremophilane, its 9-hydroxy epimer and furanopetasin: NMR and CD studies
Ladislav Novotnýa, Miloš Buděšínskýa, Josef Jizbaa, Juraj Harmathaa, Vít Lukeša, Wolfgang Lindnerb, Rolf Grosserb and Günther Snatzkeb
a Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6, Czechoslovakia
b Lehrstuhl für Strukturchemie, Ruhr-Universität Bochum, D-4630 Bochum 1, F.R.G.
Crossref Cited-by Linking
- Tori Motoo: Cumulative Data of 1H and 13C NMR Signals and Specific Rotations of Eremophilane Sesquiterpenoids. 3. 10H-Furanoeremophilanes Without 3-O Functionality. Natural Product Communications 2023, 18. <https://doi.org/10.1177/1934578X231180710>
- Siegenthaler Peter, Neuenschwander Markus: Säurekatalysierte Umlagerung von 9‐Hydroxyfuranoeremophilanen zu Eremophilanlactonen. Helvetica Chimica Acta 1996, 79, 1592. <https://doi.org/10.1002/hlca.19960790609>
- Hajós GyöRgy, Fülöp Vilmos, Kálmán Alajos, Snatzke Günther: Synthesis, X‐ray Diffraction, and CD of Cholesteno‐as‐triazines. Liebigs Ann. Chem. 1989, 1989, 25. <https://doi.org/10.1002/jlac.198919890106>
