Novel iodine-induced sulfonylation and sulfenylation of imidazopyridines have been described using sodium sulfinates as the sulfur source. This strategy enables highly selective difunctionalization of imidazo[1,2-<i>a</i>]pyridine to access sulfones and sulfides in good yields. A wide range of substrates and functional groups were well-tolerated under optimized conditions. Moreover, control experiments have been conducted, indicating a radical pathway involved in the reaction mechanisms
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
A series of low‐molecular‐weight, compact, and multifunctional cyclic alkenylsulfonyl fluorides were...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
Novel iodine-induced sulfonylation and sulfenylation of imidazopyridines have been described using s...
An efficient approach to sulfenyl imidazoheterocycles has been developed via iodine-triphenylphosphi...
An alternative method for forming sulfonates through hypervalent iodine(III) reagent-mediated oxidat...
Imidazoheterocyclic derivatives have been found to be key structural units in many natural products ...
Iodine-mediated synthesis of 3-sulfenylimidazo1{,}5-apyridines via C–H functionalization has been ac...
The advent of sulfur(VI)-fluoride exchange (SuFEx) processes as transformations with click-like reac...
Two synthetic routes to sulfondiimidamides have recently been reported. The ability to prepare and m...
The sulfonamide and N-aminosulfonamide groups are key scaffolds for both synthetic and medicinal che...
Aryl ammonium sulfinates, conveniently prepared from aryl iodides and the sulfur dioxide surrogate D...
One of the main goals of modern synthesis is to develop distinct reaction pathways from identical st...
A green, aerobic sulfenylation of imidazo[1,2-a]pyridines was performed using thiols, a flavin-and...
This thesis presents the development of novel methodologies toward the synthesis of a range of sulfo...
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
A series of low‐molecular‐weight, compact, and multifunctional cyclic alkenylsulfonyl fluorides were...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
Novel iodine-induced sulfonylation and sulfenylation of imidazopyridines have been described using s...
An efficient approach to sulfenyl imidazoheterocycles has been developed via iodine-triphenylphosphi...
An alternative method for forming sulfonates through hypervalent iodine(III) reagent-mediated oxidat...
Imidazoheterocyclic derivatives have been found to be key structural units in many natural products ...
Iodine-mediated synthesis of 3-sulfenylimidazo1{,}5-apyridines via C–H functionalization has been ac...
The advent of sulfur(VI)-fluoride exchange (SuFEx) processes as transformations with click-like reac...
Two synthetic routes to sulfondiimidamides have recently been reported. The ability to prepare and m...
The sulfonamide and N-aminosulfonamide groups are key scaffolds for both synthetic and medicinal che...
Aryl ammonium sulfinates, conveniently prepared from aryl iodides and the sulfur dioxide surrogate D...
One of the main goals of modern synthesis is to develop distinct reaction pathways from identical st...
A green, aerobic sulfenylation of imidazo[1,2-a]pyridines was performed using thiols, a flavin-and...
This thesis presents the development of novel methodologies toward the synthesis of a range of sulfo...
Sulfur functional groups are common motifs in bioactive molecules. Sulfonamides are most prevalent b...
A series of low‐molecular‐weight, compact, and multifunctional cyclic alkenylsulfonyl fluorides were...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...