An efficient thioamination of alkenes mediated by iodine(III) reagents is described. The use of different sulfur nucleophiles allows the flexible synthesis of 1,2-aminothiols from alkenes. By employing chiral iodine(III) reagents, a stereoselective version of the thioamination protocol has also been developed
Thioamides are an important, but a largely underexplored class of amide bioisostere in peptides. Rep...
A new chiral thiohydantoin catalyst is used for the stereoselective iodoamination of alkenes. N-iodo...
The sulfonamide and N-aminosulfonamide groups are key scaffolds for both synthetic and medicinal che...
Among all functional groups, alkynes occupy a privileged position in synthetic and medicinal chemist...
Chiral hypervalent iodine reagents are active players in modern stereoselective organic synthesis. S...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes h...
A thiol-alkynylation procedure utilizing the hypervalent iodine alkyne transfer reagent TIPS-ethynyl...
Hypervalent iodine compounds are molecules of increasing interest to the synthetic chemist. Their lo...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with 3 new S–X connection...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
New methodology is described to construct the olefinic bond in overcrowded alkenes using a hypervale...
Chiral hypervalent iodine compounds are used as environmentally friendly, mild, and selective oxida...
Thioamides are an important, but a largely underexplored class of amide bioisostere in peptides. Rep...
A new chiral thiohydantoin catalyst is used for the stereoselective iodoamination of alkenes. N-iodo...
The sulfonamide and N-aminosulfonamide groups are key scaffolds for both synthetic and medicinal che...
Among all functional groups, alkynes occupy a privileged position in synthetic and medicinal chemist...
Chiral hypervalent iodine reagents are active players in modern stereoselective organic synthesis. S...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with three new S-X connec...
A stereoselective hypervalent iodine-promoted oxidative rearrangement of 1,1-disubstituted alkenes h...
A thiol-alkynylation procedure utilizing the hypervalent iodine alkyne transfer reagent TIPS-ethynyl...
Hypervalent iodine compounds are molecules of increasing interest to the synthetic chemist. Their lo...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with 3 new S–X connection...
The activation of alkenes and their subsequent functionalization is a frequently used methodology in...
New methodology is described to construct the olefinic bond in overcrowded alkenes using a hypervale...
Chiral hypervalent iodine compounds are used as environmentally friendly, mild, and selective oxida...
Thioamides are an important, but a largely underexplored class of amide bioisostere in peptides. Rep...
A new chiral thiohydantoin catalyst is used for the stereoselective iodoamination of alkenes. N-iodo...
The sulfonamide and N-aminosulfonamide groups are key scaffolds for both synthetic and medicinal che...
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