Preferred Conformation of a New Ring B-Homo Diterpene, Rearrangement Product of Methyl 9α-Hydroxy-11α-Methanesulfonyloxy-(-)-Kauran-19-oate
The preferred conformation of a ring B-homo diterpene, obtained by the rearrangement of methyl 9α-hydroxy-11α-methanesulfonyloxy-(-)-kauran-10-oate 1 with potassium t-butoxide in t-butanol, was determined on the basis of the n.O.e. experiments and molecular dynamics calculations.
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Veröffentlicht in: | Natural product letters 1995-02, Vol.6 (1), p.63-68 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The preferred conformation of a ring B-homo diterpene, obtained by the rearrangement of methyl 9α-hydroxy-11α-methanesulfonyloxy-(-)-kauran-10-oate 1 with potassium t-butoxide in t-butanol, was determined on the basis of the n.O.e. experiments and molecular dynamics calculations. |
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ISSN: | 1057-5634 |
DOI: | 10.1080/10575639508044089 |