4.5 Review

Advancements in Aminofluorination of Alkenes and Alkynes: Convenient Access to β-Fluoroamines

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2015, Issue 20, Pages 4295-4309

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201500231

Keywords

Synthetic methods; Fluorine; Aminofluorination; Amines; Nitrogen heterocycles; Alkenes

Funding

  1. National Basic Research Program of China [973-2011CB808700]
  2. National Nature Science Foundation of China (NSFC) [21225210, 21202185, 21121062]
  3. Science and Technology Commission of the Shanghai Municipality [12ZR1453400]
  4. CAS/SAFEA International Partnership Program for Creative Research Teams

Ask authors/readers for more resources

Direct aminofluorination of alkenes enables the convenient synthesis of beta-fluorinated amine compounds, which are important and valuable skeletons in medicinal chemistry. In recent years this research field has received much attention and significant advancements have been made by different approaches. In this review, recently disclosed methodologies for the production of beta-fluorinated amines, based on electrophilic and metal-catalyzed processes, are summarized and discussed. Finally, the outlook and perspectives for aminofluorination are also discussed.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available