总合成的 (-) - okilactomycincin 的总合成
Amos B Smith1, Kallol Basu, Todd Bosanac
1Department of Chemistry, Laboratory for Research on the Structure of Matter, and Monell Chemical Senses Center, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA. smithab@sas.upenn.edu
Journal of the American Chemical Society
|November 14, 2007
概括
使用融合方法实现了 (-) - okilactomycin 的新型合成. 关键步骤涉及二聚体选择性 oxy-Cope 重组和 Petasis-Ferrier 联盟,以实现高效的宏观循环构造.
科学领域:
- 有机化学 有机化学
- 合成化学 合成化学
- 自然产品的合成自然产品的合成
背景情况:
- (-) - - 奥基拉克托米辛是一种复杂的天然产品,具有潜在的生物活性.
- 有效的合成路线对于访问和研究这些分子至关重要.
研究的目的:
- 开发一个高度融合和高效的合成策略,用于 (-) - okilactomycin.
- 展示复杂分子构造的关键合成转换.
主要方法:
- 灾难选择性 oxy-Cope 重组和氧化序列.
- 佩塔西斯-费里耶联盟和重新安排的战术.
- 对于宏观循环形成的环闭转化论 (RCM).
主要成果:
- 成功地执行了 (-) - okilactomycin 的高度融合合成.
- 战略级Oxy-Cope重组提供了出色的二极管选择性.
- 使用高效的RCM反应构建了13个成员的宏循环核心.
结论:
- 描述的合成路线是高效和融合的.
- 使用的方法对于复杂的宏环化合物的合成是有价值的.
- 这种合成为 (-) - okilactomycin.提供了一条可行的途径.
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