乙醇乙酸盐:用于酶选择性分子间合的多功能基质
Ji Liu1, Sourabh Mishra1, Aaron Aponick1
1Florida Center for Heterocyclic Compounds and Department of Chemistry , University of Florida , Gainesville , Florida 32611 , United States.
Journal of the American Chemical Society
|November 6, 2018
概括
一种新的 enantioselective Tsuji 化方法使用亲耳乙酸盐来创建α四分体立体中心. 这种多功能反应简化了合成,并允许快速生成具有高度的模拟物.
科学领域:
- 有机化学
- 不对称的合成
- 催化剂
背景情况:
- 津结合是有机合成中的一个基本反应.
- 选择性变异对于创造性分子至关重要.
- 之前的对抗选择性Tsuji结合方法在基质范围上存在局限性.
研究的目的:
- 开发一种多用途的反选择性分子间合.
- 为了使使用prochiral enol乙酸合成α-四分体立体中心.
- 提供快速模拟合成的融合策略.
主要方法:
- 作为基质使用了前性乙酸盐.
- 用于催化即可获得的PHOX连接物类.
- 开发了一种从氧化物中结合基的方法.
主要成果:
- 达到了高度抗选择性的Tsuji结合 (高达96% ee).
- 通过30多个例子证明了该方法的多功能性.
- 展示了Hamigeran B和新类型的快速形式合成.
结论:
- 这种方法扩大了对抗选择性Tsuji结合的范围.
- 它提供了一种强大且融合的方法来合成复杂的性分子.
- 这种反应在操作上很简单,可以容纳多种功能组.
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