酶催化环添加:合并C-C键激活和转移化合用于II型多基基结构的II型多基结构
Brett R Ambler1, Ben W H Turnbull1, Sankar Rao Suravarapu1
1University of Texas at Austin , Department of Chemistry , Austin , Texas 78712 United States.
Journal of the American Chemical Society
|July 12, 2018
概括
研究人员使用催化剂开发了一种新的enantioselective循环添加反应. 这种方法有效地产生复杂的分子,包括自然产品胺的关键部分.
科学领域:
- 有机化学 有机化学
- 催化剂是一种催化剂.
- 自然产品的合成自然产品的合成
背景情况:
- 环丁是一种多功能合成中间体.
- 酶选择性循环添加对于合成性分子至关重要.
- 金属催化C-C键形成提供了高效的合成路径.
研究的目的:
- 为了描述第一个对子环丁的酶选择性分子间金属催化循环添加.
- 开发一种方法来构建具有高立体控制的复杂多环结构.
- 为了合成"海湾地区"亚结构的 arenimycin.
主要方法:
- 使用了与 (R) -DM-SEGPHOS作为催化剂的(0) 复合物.
- 采用了通过C-C键氧化添加的分子间循环添加策略.
- 反应了四旋衍生的醇与旋丁.
主要成果:
- 首次实现了子基丁的酶选择性分子间金属催化循环添加.
- 在循环载荷管道形成中证明了完整的区域和 diastereoselectivity.
- 使用开发的催化方法获得高的选择性.
- 成功合成了 arenimycin.com 的"海湾区域".
结论:
- 开发的催化循环添加是一种强大的工具,用于enantioselective合成.
- 这种方法可以有效地访问复杂的分子架构.
- 胺基结构的合成突显了这种新反应的实用性.
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