通过催化不对称的反向化合成
Tao-Tao Gao1, Wen-Wen Zhang1, Xin Sun1
1Center of Basic Molecular Science, Department of Chemistry , Tsinghua University , Beijing , 100084 , China.
Journal of the American Chemical Society
|February 27, 2019
概括
研究人员开发了一种高度选择性的Rh催化化方法来进行有机合成. 这种新方法精确地控制立体化学,使复杂的性分子能够有效地合成药物发现和天然产品合成.
科学领域:
- 有机合成
- 催化剂
- 立体化学
背景情况:
- 在有机合成中,控制化学,区域,两极选择性和酶选择性至关重要.
- 一个分子的所有立体同位素的合成有助于天然产品的模拟合成和药物发现的奇拉化合物库的创建.
- 在多立体中心合成中精确控制相对和绝对配置仍然是不对称催化剂的挑战.
研究的目的:
- 开发一种新型的催化剂控制的化反应.
- 在合成具有多个立体中心的分子中实现前所未有的选择性.
- 提供一种多功能策略,用于基质构建块的立体分离合成.
主要方法:
- 使用皮纳科尔博兰的α,β不和碳基化合物的Rh催化化.
- 使用基质几何 (E或Z) 和配体反体 (S或R) 来控制立体化学结果.
- 由此产生的含产品的立体变化.
主要成果:
- 化反应具有较高的区域,立体和选择性.
- 在水产品中成功生成了两个邻近的立体中心.
- 通过调整基质和配体,可以轻松获得所有可能的二态异构体.
- 含的产品通过立体特异反应转化为多种性构件.
结论:
- 已经开发出一种高度选择性的催化剂控制的化.
- 这种方法提供了对多个立体中心的精确控制,解决了不对称合成的关键挑战.
- 这一策略使有价值的性化合物的高效和立体分离合成成为可能.
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