4.5 Article

Platinum-Catalyzed Substitution of Allylic Fluorides

Journal

ORGANOMETALLICS
Volume 31, Issue 4, Pages 1408-1416

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/om201029m

Keywords

-

Funding

  1. European Union [FP7-ITN-238434]
  2. MNSER
  3. CRUK
  4. EPSRC
  5. Leverhulme Trust

Ask authors/readers for more resources

Ally! fluorides are reactive toward Pt-catalyzed alkylation with malonate and likewise toward N- and O-nucleophiles under mild conditions. The reactivity of fluoride as a leaving group equals or exceeds that of the esters and carbonates commonly employed in allylic alkylation. The order of leaving-group ability with Pt catalysts was found to be F >= OCO2Me >> OBz >= OAc. This discouraged the application of platinum catalysts for the reverse reaction, fluorination of allylic substrates. Fluoride displacement involves predominant or complete retention of configuration in all the observed cases, and this was confirmed as a general feature of Pt catalysis, the stereochemical integrity being as high or higher as in Pd catalysis for the examples chosen.

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