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
A conceptionally novel nucleophilic substitution approach to synthetically important alkyl bromides ...
A new family of sulfinamide/sulfoxide derivatives was synthesized as chiral bidentate ligands by ste...
Transition metal catalyzed C-C bond and C-S bond forming reactions offer a new opportunity to constr...
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...
This thesis details the development of methods for and application of the synthesis of carbon carbon...
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...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
Pendant de nombreuses années, les liaisons C-H aliphatiques ont été considérées comme dormantes, dif...
The scientific community has born witness to incredible advancements in organic chemistry. Exemplifi...
Graduation date: 2012Sulfoxide-ligand exchange (SLE) and asymmetric halogen-metal exchange (AHME) pr...
α-Substituted oxygen-containing heterocycles are commonly present in biologically active molecules. ...
Methodology for the synthesis of enantioenriched compounds is critical to the discovery of new pharm...
A conceptionally novel nucleophilic substitution approach to synthetically important alkyl bromides ...
A new family of sulfinamide/sulfoxide derivatives was synthesized as chiral bidentate ligands by ste...
Transition metal catalyzed C-C bond and C-S bond forming reactions offer a new opportunity to constr...
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...
This thesis details the development of methods for and application of the synthesis of carbon carbon...
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...
A versatile method for the synthesis of enantioenriched N–H sulfoximines is reported. The approach s...
Pendant de nombreuses années, les liaisons C-H aliphatiques ont été considérées comme dormantes, dif...
The scientific community has born witness to incredible advancements in organic chemistry. Exemplifi...
Graduation date: 2012Sulfoxide-ligand exchange (SLE) and asymmetric halogen-metal exchange (AHME) pr...
α-Substituted oxygen-containing heterocycles are commonly present in biologically active molecules. ...
Methodology for the synthesis of enantioenriched compounds is critical to the discovery of new pharm...
A conceptionally novel nucleophilic substitution approach to synthetically important alkyl bromides ...
A new family of sulfinamide/sulfoxide derivatives was synthesized as chiral bidentate ligands by ste...
Transition metal catalyzed C-C bond and C-S bond forming reactions offer a new opportunity to constr...