<div><p>ABSTRACT</p><p>Described in this work is a catalyst free, in most cases neat, preparation of heterocyclic thienyl sulfides. This method utilizes 2-thiophenethiol and various activated halogenated heterocycles in a substitution type reaction to form an interesting array of sulfides. Yields obtained are comparable other published methods and require milder conditions, shorter reaction times and most times eliminates the need for column chromatography during work-up.</p></div
Iodine-catalyzed direct arylthiation of substituted anilines for the synthesis of various diaryl sul...
Three component reactions of olefins, amines, and sulfur were studied. Thioamidation of styrenes is ...
A mild and odorless copper-catalyzed thiolation of terminal alkynes with thiosulfonates is described...
Metal-free C–H thioarylation of arenes and heteroarenes using methyl sulfoxides constitutes a genera...
Thiophene derivatives have been prepared by means of a functionalized imidazolium salt [1,3‐bis(carb...
Alumina-supported copper sulfate efficiently catalyzes the S-arylation of aromatic, heteroaromatic a...
A convenient one-pot approach for the synthesis of aryl sulfides through the coupling of thiols with...
A new protocol for the one-pot synthesis of styryl alkyl sulfides was developed. This methodology in...
ABSTRACT: A mild protocol for the synthesis of diaryl and heteroaryl sulfides is described. In a one...
An operationally simple, practical, and efficient cascade approach employing α-allyl dithioesters an...
A convenient synthesis of aromatic sulfides which are obtained cleany and in generally eccellent yie...
The work covers the aromatic, heteroaromatic and aliphatic allyl sulfides and esters. The aim is to ...
International audienceWe provide efficient synthetic access to heteroaryl sulfones in two-steps usin...
In this paper, we report an efficient synthetic method for thioester formation from sodium thiosulfa...
As a model study, a series of linear and branched p-phenylene and m- phenylene sulfides, functionali...
Iodine-catalyzed direct arylthiation of substituted anilines for the synthesis of various diaryl sul...
Three component reactions of olefins, amines, and sulfur were studied. Thioamidation of styrenes is ...
A mild and odorless copper-catalyzed thiolation of terminal alkynes with thiosulfonates is described...
Metal-free C–H thioarylation of arenes and heteroarenes using methyl sulfoxides constitutes a genera...
Thiophene derivatives have been prepared by means of a functionalized imidazolium salt [1,3‐bis(carb...
Alumina-supported copper sulfate efficiently catalyzes the S-arylation of aromatic, heteroaromatic a...
A convenient one-pot approach for the synthesis of aryl sulfides through the coupling of thiols with...
A new protocol for the one-pot synthesis of styryl alkyl sulfides was developed. This methodology in...
ABSTRACT: A mild protocol for the synthesis of diaryl and heteroaryl sulfides is described. In a one...
An operationally simple, practical, and efficient cascade approach employing α-allyl dithioesters an...
A convenient synthesis of aromatic sulfides which are obtained cleany and in generally eccellent yie...
The work covers the aromatic, heteroaromatic and aliphatic allyl sulfides and esters. The aim is to ...
International audienceWe provide efficient synthetic access to heteroaryl sulfones in two-steps usin...
In this paper, we report an efficient synthetic method for thioester formation from sodium thiosulfa...
As a model study, a series of linear and branched p-phenylene and m- phenylene sulfides, functionali...
Iodine-catalyzed direct arylthiation of substituted anilines for the synthesis of various diaryl sul...
Three component reactions of olefins, amines, and sulfur were studied. Thioamidation of styrenes is ...
A mild and odorless copper-catalyzed thiolation of terminal alkynes with thiosulfonates is described...