15. Copper-Catalyzed Trifluoromethylation of Allylic Bromodifluoroacetic Esters

 
 

Ambler, B. R.; Altman, R. A.*

Org. Lett. 2013, 15, 5578–5581.

The development of new synthetic fluorination reactions has important implications in medicinal, agricultural, and materials chemistries. Given the prevalence and accessibility of alcohols, methods to convert alcohols to trifluoromethanes are desirable. However, this transformation typically requires four-step processes, specialty chemicals, and/or stoichiometric metals to access the trifluoromethyl-containing product. A two-step copper-catalyzed decarboxylative protocol for converting allylic alcohols to trifluoromethanes is reported. Preliminary mechanistic studies distinguish this reaction from previously reported Cu-mediated reactions.

Previous
Previous

16. Decarboxylative Fluorination Strategies for Accessing Medicinally-Relevant Products

Next
Next

14. Copper-Mediated Deoxygenative Trifluoromethylation of Benzylic Xanthates: Formation of C(sp3)–CF3 from an O-Based Electrophile