维里丁和维里迪奥尔的总合成
Yang Ji1, Zhengyuan Xin1, Haibing He2
1Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering , East China Normal University , 3663N Zhongshan Road , Shanghai 200062 , China.
Journal of the American Chemical Society
|September 27, 2019
概括
研究人员实现了抗真菌化合物 (-) - 维里丁和 (-) - 维里的总合成. 这种可扩展的方法利用了金属化物H原子转移 (MHAT) 激素循环等关键反应进行潜在的生物研究.
科学领域:
- 有机化学
- 合成化学
- 自然产品化学
背景情况:
- 维里丁和维里迪奥是复杂结构的抗真菌代谢物.
- 生物评估和进一步研究需要有效的合成途径.
研究的目的:
- 为了实现 (-) - 维里丁和 (-) - 维里的不对称总合成.
- 开发一个可扩展和融合的合成策略.
主要方法:
- 使用l-ribose衍生物构建D环的分子内 [3+2] 循环添加.
- 同催化金属化物H原子转移 (MHAT) 激素循环,用于C环形成和四元中心安装.
- 融合合成的战略.
主要成果:
- 在17个步骤中合成 (-) - 维里丁.
- 在18个步骤中合成的 (-) - 乙.
- 成功构建了关键的性三片段和全碳四元中心.
结论:
- 已经确定了可扩展的 (-) - 维里丁和 (-) - 维里的总合成.
- 开发的策略为生物研究获得这些抗真菌代谢物提供了可行的途径.
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