Metal-free C–H thioarylation of arenes and heteroarenes using methyl sulfoxides constitutes a general protocol for the synthesis of high value diaryl sulfides. The coupling of arenes and heteroarenes with in situ activated sulfoxides is regioselective, uses readily available starting materials, is operationally simple, and tolerates a wide range of functional groups
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...
A transition-metal-free arylation of sulfenate anions generated from β-sulfinyl esters with diarylio...
A simple, efficient, and practical metal-free C–H sulfenylation of substituted electron-rich arenes ...
Arenes react smoothly with thionyl chloride in the presence of a catalytic amount of scandium trifla...
<div><p>ABSTRACT</p><p>Described in this work is a catalyst free, in most cases neat, preparation of...
A metal-free CH–CH-type coupling of arenes and alkynes, mediated by a multifunctional sulfoxide dire...
ABSTRACT: A mild protocol for the synthesis of diaryl and heteroaryl sulfides is described. In a one...
A novel, atom economical, and transition-metal-free strategy for the synthesis of thiophenes from su...
Rhodium-catalyzed sulfonylation, thioetherification, thiocyanation, and other heterofunctionalizatio...
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomericall...
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomericall...
An efficient, high-yielding, and transition-metal-free synthesis of diaryl sulfones from arylsulfini...
International audienceWe provide efficient synthetic access to heteroaryl sulfones in two-steps usin...
We have developed metal-free regiocontrolled dehydrogenative C–H/C–H cross-coupling of aryl sulfoxid...
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...
A transition-metal-free arylation of sulfenate anions generated from β-sulfinyl esters with diarylio...
A simple, efficient, and practical metal-free C–H sulfenylation of substituted electron-rich arenes ...
Arenes react smoothly with thionyl chloride in the presence of a catalytic amount of scandium trifla...
<div><p>ABSTRACT</p><p>Described in this work is a catalyst free, in most cases neat, preparation of...
A metal-free CH–CH-type coupling of arenes and alkynes, mediated by a multifunctional sulfoxide dire...
ABSTRACT: A mild protocol for the synthesis of diaryl and heteroaryl sulfides is described. In a one...
A novel, atom economical, and transition-metal-free strategy for the synthesis of thiophenes from su...
Rhodium-catalyzed sulfonylation, thioetherification, thiocyanation, and other heterofunctionalizatio...
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomericall...
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomericall...
An efficient, high-yielding, and transition-metal-free synthesis of diaryl sulfones from arylsulfini...
International audienceWe provide efficient synthetic access to heteroaryl sulfones in two-steps usin...
We have developed metal-free regiocontrolled dehydrogenative C–H/C–H cross-coupling of aryl sulfoxid...
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...
A transition-metal-free arylation of sulfenate anions generated from β-sulfinyl esters with diarylio...