| Journal of the Brazilian Chemical Society | |
| Preparation of (5R)-4,8-dimethylbicyclo[3.3.0]oct-1(8),3-dien-2-one from (-)-limonene oxide: a novel intermediate to the synthesis of 4-5-5 fused tricarbocyclic core present in terpenic natural products | |
| Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil1  Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil1  Ceschi, Marco A.1  Pisoni, Diego S.1  Silva, Daniel B.1  Schenato, Rossana A.1  | |
| 关键词: limonene oxide; bicyclo[3.3.0]octane; chiral; building block; | |
| DOI : 10.1590/S0103-50532004000500007 | |
| 学科分类:化学(综合) | |
| 来源: SciELO | |
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【 摘 要 】
This paper describes the conversion of the readily available (-)-limonene oxide to the new (5R)-4,8-dimethylbicyclo[3.3.0]oct-1(8),3-dien-2-one. This compound holds the prospect of serving as a useful chiral building block or intermediate to prepare a variety of compounds having a bicyclo[3.3.0]octane framework. The synthetic strategy made use of the umpolung reactivity of cyanohydrin TMS ether, as an acyl anion equivalent, in order to promote intramolecular alkylation. The formal synthesis of (-)-kelsoene was achieved by preparing a known advanced intermediate (1R,5S,8R)-4,8-dimethylbicyclo[3.3.0]oct-3-en-2-one via selective hydrogenation of the named compound (5R)-4,8-dimethylbicyclo[3.3.0]oct-1(8),3-dien-2-one.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912050579583ZK.pdf | 224KB |
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