The radical azidoalkylation of alkenes that was initially developed with α-iodoesters and α-iodoketones was extended to other activated iodomethyl derivatives. By using iodomethyl aryl sulfones, the preparation of γ-azidosulfones was easily achieved. Facile conversion of these azidosulfones to homoallylic azides using a Julia–Kocienski olefination reaction is reported, making the whole process equivalent to the azidoalkenylation of terminal alkenes
A transition metal-free strategy for the dehydrogenative β-sulfonylation of tertiary cyclic amines i...
An unprecedented set of structurally diverse sulfonimidamides (47?compounds) has been prepared by va...
Dichloroindium hydride revealed to be a valid alternative to tributyltin hydride for radical reduct...
Recent advances in radical azidation using sulfonyl azides are presented. For instance, radical carb...
A versatile synthesis of azidolactones through azidation and cyclization of carboxylic acids onto al...
The oxidative oligoazidation of phenols and ketones using iodine azide (IN3) provided by its release...
The generation of sulfonyl radicals from sulfonyl azides using visible light and a photoactive iridi...
Two previously unknown protocols for Pd-catalyzed allylic C-H sulfonylation of terminal alkenes have...
The reaction of aryl iodides, N‐tert‐butanesulfinamide, and allyl or homoallyl alcohol in the presen...
An aza-Peterson olefination methodology to access 1,3-dienes and stilbene derivatives from the corre...
Electron-rich aza-aromatic compounds such as indoles and pyrroles represent systems of particular in...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
An N-heterocyclic carbene promotes cyclization of sulfonylalkynols and sulfonylalkynamides that acco...
We recently reported two unexplored reactivities of alkynes and azides. The first method reacts nuc...
A transition metal-free strategy for the dehydrogenative β-sulfonylation of tertiary cyclic amines i...
An unprecedented set of structurally diverse sulfonimidamides (47?compounds) has been prepared by va...
Dichloroindium hydride revealed to be a valid alternative to tributyltin hydride for radical reduct...
Recent advances in radical azidation using sulfonyl azides are presented. For instance, radical carb...
A versatile synthesis of azidolactones through azidation and cyclization of carboxylic acids onto al...
The oxidative oligoazidation of phenols and ketones using iodine azide (IN3) provided by its release...
The generation of sulfonyl radicals from sulfonyl azides using visible light and a photoactive iridi...
Two previously unknown protocols for Pd-catalyzed allylic C-H sulfonylation of terminal alkenes have...
The reaction of aryl iodides, N‐tert‐butanesulfinamide, and allyl or homoallyl alcohol in the presen...
An aza-Peterson olefination methodology to access 1,3-dienes and stilbene derivatives from the corre...
Electron-rich aza-aromatic compounds such as indoles and pyrroles represent systems of particular in...
Sulfonimidamides are intriguing new motifs for medicinal and agrochemistry, and provide attractive b...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
An N-heterocyclic carbene promotes cyclization of sulfonylalkynols and sulfonylalkynamides that acco...
We recently reported two unexplored reactivities of alkynes and azides. The first method reacts nuc...
A transition metal-free strategy for the dehydrogenative β-sulfonylation of tertiary cyclic amines i...
An unprecedented set of structurally diverse sulfonimidamides (47?compounds) has been prepared by va...
Dichloroindium hydride revealed to be a valid alternative to tributyltin hydride for radical reduct...