4.8 Article

Nickel-Catalyzed Amination of Aryl Sulfamates and Carbamates Using an Air-Stable Precatalyst

期刊

ORGANIC LETTERS
卷 14, 期 16, 页码 4182-4185

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ol301847m

关键词

-

资金

  1. Boehringer Ingelheim
  2. DuPont
  3. Eli Lilly
  4. Amgen
  5. AstraZeneca
  6. Roche
  7. A. P. Sloan Foundation
  8. Foote family (fellowship)
  9. University of California, Los Angeles
  10. NSF [CHE-1048804]
  11. National Center for Research Resources [S10RR025631]
  12. Direct For Mathematical & Physical Scien [1048804] Funding Source: National Science Foundation
  13. Division Of Chemistry [1048804] Funding Source: National Science Foundation

向作者/读者索取更多资源

A facile nickel-catalyzed method to achieve the amination of synthetically useful aryl sulfamates and carbamates is reported. Contrary to most Ni-catalyzed amination reactions, this user-friendly approach relies on an air-stable Ni(II) precatalyst, which, when employed with a mild reducing agent, efficiently delivers aminated products in good to excellent yields. The scope of the method is broad with respect to both coupling partners and includes heterocyclic substrates.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据