In this work we report a new synthetic tactic for the straightforward preparation of hardly accessible sulfinamidines and sulfinamide esters, by using a simple metal-free protocol. The process is robust and uses readily available sulfenamides as the S-donor and sulfonyloxycarbamates as the N-source. The scope and mechanism have also been investigated
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
A new N-silyl sulfinylamine reagent allows the rapid preparation of a broad range of (hetero)aryl, a...
Sulfondiimines are marginalized entities among nitrogencontaining organosulfur compounds, despite of...
In this work we report a new synthetic tactic for the straightforward preparation of hardly accessib...
Metal- and additive-free transsulfinamidation of N-unsubstituted sulfinamides and N-pivaloyl-protect...
In this work we investigated, for the first time, the reactivity of sulfinimidate esters as an elect...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
Sulfoximines are emerging as valuable new isosteres for use in medicinal chemistry, with the potenti...
The development of NH transfer reactions using hypervalent iodine and simple sources of ammonia has ...
Sulfoximines are emerging as valuable new isosteres for use in medicinal chemistry, with the potenti...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S–X connec...
Sulfonimidamides were prepared in a one-pot transformation from sulfonamides, through nucleophilic s...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with 3 new S–X connection...
Sulfonylureas are employed in a variety of applications including use as drugs to treat type II diab...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
A new N-silyl sulfinylamine reagent allows the rapid preparation of a broad range of (hetero)aryl, a...
Sulfondiimines are marginalized entities among nitrogencontaining organosulfur compounds, despite of...
In this work we report a new synthetic tactic for the straightforward preparation of hardly accessib...
Metal- and additive-free transsulfinamidation of N-unsubstituted sulfinamides and N-pivaloyl-protect...
In this work we investigated, for the first time, the reactivity of sulfinimidate esters as an elect...
In the following thesis, new methodologies which exploit sulfinylamine reagents to enable one-pot sy...
Sulfoximines are emerging as valuable new isosteres for use in medicinal chemistry, with the potenti...
The development of NH transfer reactions using hypervalent iodine and simple sources of ammonia has ...
Sulfoximines are emerging as valuable new isosteres for use in medicinal chemistry, with the potenti...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S–X connec...
Sulfonimidamides were prepared in a one-pot transformation from sulfonamides, through nucleophilic s...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with 3 new S–X connection...
Sulfonylureas are employed in a variety of applications including use as drugs to treat type II diab...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
A new N-silyl sulfinylamine reagent allows the rapid preparation of a broad range of (hetero)aryl, a...
Sulfondiimines are marginalized entities among nitrogencontaining organosulfur compounds, despite of...