Sulfonimidamides are an emerging bioisosteric replacement in medicinal chemistry projects, and therefore new chemistries are necessary to access this functionality. The general synthesis of CF3-sulfonimidamides from an activated bench-stable transfer reagent is described. A diverse reaction scope is demonstrated, with a wide range of nucleophilic amines being tolerated in this transformation. The CF3-sulfonimidamides obtained contain an additional diversity point, in the form a protected imine, that could be unmasked to allow late stage modifications
Two synthetic routes to sulfondiimidamides have recently been reported. The ability to prepare and m...
The CF3SN moiety is a substituent with interesting properties. However, there is no easy synthetic a...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
Sulfonimidamides are an emerging bioisosteric replacement in medicinal chemistry projects, and there...
Sulfonimidamides are an emerging bioisosteric replacement in medicinal chemistry projects, and there...
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
A method using calcium triflimide [Ca(NTf2)2] as a Lewis acid to activate sulfonyl fluorides toward ...
Sulfonimidamides were prepared in a one-pot transformation from sulfonamides, through nucleophilic s...
A new N-silyl sulfinylamine reagent allows the rapid preparation of a broad range of (hetero)aryl, a...
Sulfonimidamides are increasingly important molecules in medicinal chemistry and agrochemistry, but ...
A method using calcium triflimide [Ca(NTf<sub>2</sub>)<sub>2</sub>] as a Lewis acid to activate sul...
Due to their three-dimensional structure, chemical and metabolic stability, polarity, and hydrogen-b...
Sulfonimidamides are increasingly important molecules in medicinal chemistry and agrochemistry, but ...
Sulfoximines, the monoaza analogues of sulfones, have recently gained considerable recognition as a ...
The development of NH transfer reactions using hypervalent iodine and simple sources of ammonia has ...
Two synthetic routes to sulfondiimidamides have recently been reported. The ability to prepare and m...
The CF3SN moiety is a substituent with interesting properties. However, there is no easy synthetic a...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
Sulfonimidamides are an emerging bioisosteric replacement in medicinal chemistry projects, and there...
Sulfonimidamides are an emerging bioisosteric replacement in medicinal chemistry projects, and there...
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
A method using calcium triflimide [Ca(NTf2)2] as a Lewis acid to activate sulfonyl fluorides toward ...
Sulfonimidamides were prepared in a one-pot transformation from sulfonamides, through nucleophilic s...
A new N-silyl sulfinylamine reagent allows the rapid preparation of a broad range of (hetero)aryl, a...
Sulfonimidamides are increasingly important molecules in medicinal chemistry and agrochemistry, but ...
A method using calcium triflimide [Ca(NTf<sub>2</sub>)<sub>2</sub>] as a Lewis acid to activate sul...
Due to their three-dimensional structure, chemical and metabolic stability, polarity, and hydrogen-b...
Sulfonimidamides are increasingly important molecules in medicinal chemistry and agrochemistry, but ...
Sulfoximines, the monoaza analogues of sulfones, have recently gained considerable recognition as a ...
The development of NH transfer reactions using hypervalent iodine and simple sources of ammonia has ...
Two synthetic routes to sulfondiimidamides have recently been reported. The ability to prepare and m...
The CF3SN moiety is a substituent with interesting properties. However, there is no easy synthetic a...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...