The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomerically pure diarylalkanes in up to 98% yield and greater than 99.5% enantiomeric excess. This ligand coupling reaction is tolerant to multiple substitution patterns and provides access to diverse areas of chemical space in three operationally simple steps from commercially available reagents. This strategy provides orthogonal access to electron-deficient heteroaromatic compounds, traditionally synthesised via transition metal-catalysed cross-couplings, which circumvents common issues associated with proto-demetalation and β-hydride elimination
Metal-free C–H thioarylation of arenes and heteroarenes using methyl sulfoxides constitutes a genera...
A novel approach to produce chiral diaryl sulfoxides from aryl benzyl sulfoxides and aryl bromides v...
The enantioselective 1,1-diarylation of allyl sulfones and vinyl sulfones is reported for the first ...
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...
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomericall...
PART I: Chemists are relentlessly searching for innovative approaches to activate the least reactive...
PART I: Chemists are relentlessly searching for innovative approaches to activate the least reactive...
Over the decades, non-activated C-H bonds have been considered as dormant functionalities, hardly ex...
Although chiral sulfoxides are important motifs in medicinal chemistry and asymmetric synthesis, des...
This thesis details the development of methods for and application of the synthesis of carbon carbon...
Methodology for the synthesis of enantioenriched compounds is critical to the discovery of new pharm...
The scientific community has born witness to incredible advancements in organic chemistry. Exemplifi...
The palladium-catalyzed coupling of enantiopure 2-halovinylsulfoxides and (E)-vinyl stannanes procee...
An efficient Rh-catalyzed addition of arylboronic acids to N-tosylarylimines has been developed with...
Metal-free C–H thioarylation of arenes and heteroarenes using methyl sulfoxides constitutes a genera...
A novel approach to produce chiral diaryl sulfoxides from aryl benzyl sulfoxides and aryl bromides v...
The enantioselective 1,1-diarylation of allyl sulfones and vinyl sulfones is reported for the first ...
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...
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomericall...
PART I: Chemists are relentlessly searching for innovative approaches to activate the least reactive...
PART I: Chemists are relentlessly searching for innovative approaches to activate the least reactive...
Over the decades, non-activated C-H bonds have been considered as dormant functionalities, hardly ex...
Although chiral sulfoxides are important motifs in medicinal chemistry and asymmetric synthesis, des...
This thesis details the development of methods for and application of the synthesis of carbon carbon...
Methodology for the synthesis of enantioenriched compounds is critical to the discovery of new pharm...
The scientific community has born witness to incredible advancements in organic chemistry. Exemplifi...
The palladium-catalyzed coupling of enantiopure 2-halovinylsulfoxides and (E)-vinyl stannanes procee...
An efficient Rh-catalyzed addition of arylboronic acids to N-tosylarylimines has been developed with...
Metal-free C–H thioarylation of arenes and heteroarenes using methyl sulfoxides constitutes a genera...
A novel approach to produce chiral diaryl sulfoxides from aryl benzyl sulfoxides and aryl bromides v...
The enantioselective 1,1-diarylation of allyl sulfones and vinyl sulfones is reported for the first ...