基因的Enantio-和区域选择性CuH催化胺化
Shaolin Zhu1, Nootaree Niljianskul, Stephen L Buchwald
1Department of Chemistry, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
一种新型的铜催化反应使基的抗选择性胺化成为可能,从烯中产生有价值的α分支氨基和从亚利法性基中产生抗马尔科夫尼科夫产物.
科学领域:
- 有机化学 有机化学
- 催化剂是一种催化剂.
- 合成方法论 合成方法论
背景情况:
- 基的胺化是合成含化合物的关键转化.
- 开发enantioselective和regioselective方法仍然是有机合成的一个重大挑战.
研究的目的:
- 开发一种新的铜催化胺化反应.
- 在反应中实现高的enantio和regioselectivity.
- 为了探索各种替代的反应范围.
主要方法:
- 使用铜催化剂系统与二氧化甲基和基胺.
- 研究了与一系列替代烯 (转基,基和β,β-非替代) 的反应.
- 检查了与阿利法性烯的反应.
主要成果:
- 实现了高和区域选择性的铜催化氨酸的化.
- 从各种替代的烯中成功合成α分支胺.
- 从亚利法性烯中产生的完全抗马尔科夫尼科夫的胺化产品.
结论:
- 开发的方法提供了一条有效的途径,以致于以酶体丰富的α-分支氨基.
- 该反应证明了对各种基底的广泛适用性.
- 这项工作扩大了通过胺化选择性氨基合成的工具包.
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