通过弱协调基组辅助的高选择性催化氧化碳循环
Daniels Posevins1, Youai Qiu1, Jan-E Bäckvall1
1Department of Organic Chemistry, Arrhenius Laboratory , Stockholm University , SE-106 91 Stockholm , Sweden.
Journal of the American Chemical Society
|February 10, 2018
概括
一种新的催化反应使得从乙烯中合成功能化环醇衍生物. 这种方法提供了对立体化学的高度控制,利用基组来指导反应途径.
科学领域:
- 有机化学
- 催化剂
- 合成方法
背景情况:
- 催化反应对于C-C键的形成至关重要.
- 开发复杂分子合成的二元选择性方法仍然是一个挑战.
研究的目的:
- 开发一种新型的催化氧化碳循环-化.
- 在形成循环烯醇衍生物时实现高二选择性.
主要方法:
- 使用催化剂进行氧化碳循环-化.
- 使用弱协调基来指导反应.
- 研究涉及连接物交换和氨酸协调的机制.
主要成果:
- 通过控制的1,3-相对立体化学 (d.r. >50:1) 的情况.
- 证明其他含氧组 (,氧化物,乙酸盐) 也可以促进碳循环.
- 确定了接近含氧功能的必要性,以确保反应的成功.
结论:
- 已经开发出一种高度分离选择的催化反应,用于烯功能化.
- 基团在通过面部选择性协调指导立体化学方面发挥着关键作用.
- 这种方法为构建复杂的循环结构提供了强大的工具.
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