4.8 Article

Isocyanide Insertion: De Novo Synthesis of Trifluoromethylated Phenanthridine Derivatives

Journal

ORGANIC LETTERS
Volume 15, Issue 21, Pages 5520-5523

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol4026827

Keywords

-

Funding

  1. National Basic Research Program of China [2011CB935800]
  2. 863 program [2013AA092903]
  3. National Natural Science Foundation of China [21121091, 21102072]
  4. Natural Science Foundation of Jiangsu Province [BK2012012, BK20131266]

Ask authors/readers for more resources

A mechanistically new strategy has been described for the simple, practical, and environmentally friendly preparation of 6-(trifluoromethyl)phenanthridine derivatives using ionic isocyanide insertion from biphenyl isocyanide derivatives and Umemoto's reagent. These reactions were promoted only by inorganic base in good-to-excellent chemical yields without any external stoichiometric oxidants and radical initiators.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available