Herein we disclose an efficient method for the conversion of carboxylic acids to trifluoromethyl groups via the combination of photoredox and copper catalysis. This transformation tolerates a wide range of functionality including heterocycles, olefins, alcohols, and strained ring systems. To demonstrate the broad potential of this new methodology for late-stage functionalization, we successfully converted a diverse array of carboxylic acid-bearing natural products and medicinal agents to the corresponding trifluoromethyl analogues
The direct conversion of aliphatic carboxylic acids to the corresponding alkyl fluorides has been ac...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...
Polyfluoroarenes are useful building blocks in several areas such as drug discovery, materials, and ...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
Carboxylic acids are one of the most suitable starting materials for synthesis. They are readily ava...
Selective copper catalyzed activation of ketoacids and notably bio-sourced 1,3-acetonedicarboxylic a...
Aliphatic carboxylic acids exist widely in nature and serve as an attractive feedstock in organic sy...
Aliphatic carboxylic acids exist widely in nature and serve as an attractive feedstock in organic sy...
Polyfluoroarenes are an important class of compounds in medical and material chemistry. The synthesi...
A scalable and operationally simple decarboxylative trifluoromethylation of (hetero)arenes with eas...
We report a photoinduced iron/copper dual-catalytic strategy for the radical decarboxylation functio...
Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid s...
An efficient copper-catalyzed trifluoromethylation of polysubstituted alkenes assisted by decarboxyl...
The development of efficient methods for accessing fluorinated functional groups is desirable. Herei...
The direct conversion of aliphatic carboxylic acids to the corresponding alkyl fluorides has been ac...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...
Polyfluoroarenes are useful building blocks in several areas such as drug discovery, materials, and ...
The development of new synthetic fluorination reactions has important implications in medicinal, agr...
Carboxylic acids are one of the most suitable starting materials for synthesis. They are readily ava...
Selective copper catalyzed activation of ketoacids and notably bio-sourced 1,3-acetonedicarboxylic a...
Aliphatic carboxylic acids exist widely in nature and serve as an attractive feedstock in organic sy...
Aliphatic carboxylic acids exist widely in nature and serve as an attractive feedstock in organic sy...
Polyfluoroarenes are an important class of compounds in medical and material chemistry. The synthesi...
A scalable and operationally simple decarboxylative trifluoromethylation of (hetero)arenes with eas...
We report a photoinduced iron/copper dual-catalytic strategy for the radical decarboxylation functio...
Trifluoromethanes play an important role in medicinal chemistry, and methods that enable the rapid s...
An efficient copper-catalyzed trifluoromethylation of polysubstituted alkenes assisted by decarboxyl...
The development of efficient methods for accessing fluorinated functional groups is desirable. Herei...
The direct conversion of aliphatic carboxylic acids to the corresponding alkyl fluorides has been ac...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...
Trifluoroethylarenes are found in a variety of biologically active molecules, and strategies for acc...