Inhaltsstoffe des Osmanthus-Absolues 6. Mitteilung. (7S, 10S, 5E)- und (7R, 10S, 5E)-2,6,10-Trimethyl-7,10-epoxy-2,5,11-dodecatrien
✍ Scribed by Roman Kaiser; Dietmar Lamparsky
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- German
- Weight
- 419 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Constituents of Osmanthus Absolute, 6th Communication. (7**S, 10S, 5E)‐ and (7****R, 10S, 5E****)‐2,6,10‐Trimethyl‐7,10‐epoxy‐2,5,11‐dodecatriene**
Two novel sesquiterpenoid oxides 1a and 1b from Osmanthus absolute have been identified. Their structural proof is based on pectral data and synthesis starting from the known methyl [5‐methyl‐5‐vinyl‐tetrahydrofur‐1‐yl] ketones (4a and 4b, respectively), whose configuration is well established. The thus obtained compounds 1a/1b identical with the natural products, were accompanied by their corresponding 6‐methylidene isomers 3a and 3b which could not be detected in the natural substrate.
📜 SIMILAR VOLUMES
Hydrogenation of the ketone group in di-0-benzylderivative (8) of the known macrocyclic lactone zeralenone (7) using a novel chiral borane complex 3.BH3, prepared in situ, proceeded at lower temperatures with moderate diastereoselectivity ( -40%, d.e. at -60"). Unsaturated diastereomers 9 and 10 wer
## Abstract The synthesis of hexabenz‐1,12;2,3;4,5;6,7;8,9;10,11‐coronene, using two different reaction schemes is described. The cyclodehydrogenation of hexaphenylbenzene, and the reaction of dibenz‐1,9;2,3‐anthrone with Zn/ZnCl~2~ lead to identical products, the chemical and crystallographic prop