A novel molecular iodine-catalyzed protocol for the construction of thiocarbamates from readily available sodium sulfinates, isocyanides, and water has been described. The present methodology offers a facile and practical route to a variety of thiocarbamates in moderate to good yields with favorable functional group tolerance by use odorless sodium sulfinates as the sulfur source. The mechanistic studies suggest the present transformation involves a radical process
An efficient synthesis of sulfonyl carbamates and sulfonyl ureas from sulfonyl azides employing a pa...
Catalyst-free conjugate addition of thiols to α,β-unsaturated carbonyl compounds in water is reporte...
An improved method for the selenium-catalysed synthesis of thiocarbamates under mild conditions has ...
An efficient isocyanide-based synthesis of S-thiocarbamates was discovered and thoroughly investigat...
Thiocarbamates, a type of compounds containing many functional groups and possessing bioactivity, ha...
A convenient visible-light-induced method for the synthesis of thiocarbamates from isocyanides, thio...
In this work we report a new synthetic tactic for the straightforward preparation of hardly accessib...
In this paper, we report an efficient synthetic method for thioester formation from sodium thiosulfa...
A convenient, efficient and green procedure for the synthesis of S-aryl dithiocarbamates has been de...
Silica sulfuric acid catalyzes efficiently the reaction of carbamates and oxazolidinones with anhydr...
A novel, efficient, and regioselective transition-metal-free one-pot synthesis of aryl sulfones via ...
Isothiocyanates (ITCs) are biologically active molecules found in several natural products and pharm...
Sulfonyl-derived functional groups populate a broad range of useful molecules and materials, and des...
We report the facile and efficient metal-free metathesis reaction of <i>C</i>-chiral allylic sulfili...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with 3 new S–X connection...
An efficient synthesis of sulfonyl carbamates and sulfonyl ureas from sulfonyl azides employing a pa...
Catalyst-free conjugate addition of thiols to α,β-unsaturated carbonyl compounds in water is reporte...
An improved method for the selenium-catalysed synthesis of thiocarbamates under mild conditions has ...
An efficient isocyanide-based synthesis of S-thiocarbamates was discovered and thoroughly investigat...
Thiocarbamates, a type of compounds containing many functional groups and possessing bioactivity, ha...
A convenient visible-light-induced method for the synthesis of thiocarbamates from isocyanides, thio...
In this work we report a new synthetic tactic for the straightforward preparation of hardly accessib...
In this paper, we report an efficient synthetic method for thioester formation from sodium thiosulfa...
A convenient, efficient and green procedure for the synthesis of S-aryl dithiocarbamates has been de...
Silica sulfuric acid catalyzes efficiently the reaction of carbamates and oxazolidinones with anhydr...
A novel, efficient, and regioselective transition-metal-free one-pot synthesis of aryl sulfones via ...
Isothiocyanates (ITCs) are biologically active molecules found in several natural products and pharm...
Sulfonyl-derived functional groups populate a broad range of useful molecules and materials, and des...
We report the facile and efficient metal-free metathesis reaction of <i>C</i>-chiral allylic sulfili...
Aryl thiols can be selectively converted to sulfonimidates or sulfonamides with 3 new S–X connection...
An efficient synthesis of sulfonyl carbamates and sulfonyl ureas from sulfonyl azides employing a pa...
Catalyst-free conjugate addition of thiols to α,β-unsaturated carbonyl compounds in water is reporte...
An improved method for the selenium-catalysed synthesis of thiocarbamates under mild conditions has ...