利特拉辛B的总合成
Yasuaki Nakayama1, Michael R Maser1, Tatsuya Okita1
1The Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.
Journal of the American Chemical Society
|March 10, 2021
概括
研究人员报告了细胞毒性化物Ritterazine B的首次完全合成. 这项研究介绍了类固醇子单元的统一策略,利用关键的和黄金催化反应进行高效的构建.
科学领域:
- 有机化学
- 自然产品合成
- 医学化学
背景情况:
- 里特拉B是一种细胞毒性类化合物,具有潜在的治疗用途.
- 里特拉B的复杂结构带来了重要的合成挑战.
- 之前没有报道过合成路径到Ritterazine B或其类似物.
研究的目的:
- 为了实现细胞毒性化物Ritterazine B的首次全合成.
- 开发一个统一和高效的合成策略来构建类固醇子单元.
- 探索用于安装关键结构特征的新型合成方法.
主要方法:
- 一个统一的方法,从一个共同的先驱体的类固醇子单位.
- 用为媒介进行散合成.
- 黄金催化循环异构,用于螺旋形成.
- 晚期C-H氧化用于酒精合并.
主要成果:
- 成功的整体合成利特拉B.
- 展示一个统一的策略来组装类固醇子单元.
- 有效地安装螺旋和C7'酒精.
结论:
- 报告的合成提供了一个可行的路径,以Ritterazine B.
- 开发的方法可用于合成相关的天然产品.
- 这项工作扩大了复杂分子合成的工具包.
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