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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| container_end_page | 68 |
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| container_issue | 1 |
| container_start_page | 63 |
| container_title | Natural product letters |
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| creator | Nakano, Tatsuhiko Maillo, María Aracelis Usubillaga, Alfredo Troconis, Mary Cordero De |
| description | 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. |
| doi_str_mv | 10.1080/10575639508044089 |
| format | Article |
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| identifier | ISSN: 1057-5634 |
| ispartof | Natural product letters, 1995-02, Vol.6 (1), p.63-68 |
| issn | 1057-5634 |
| language | eng |
| recordid | cdi_crossref_primary_10_1080_10575639508044089 |
| source | Taylor & Francis:Master (3349 titles) |
| subjects | a ring B-homo kaurane derivative molecular dynamics calculations n.O.e preferred conformation |
| title | Preferred Conformation of a New Ring B-Homo Diterpene, Rearrangement Product of Methyl 9α-Hydroxy-11α-Methanesulfonyloxy-(-)-Kauran-19-oate |
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