An asymmetric Ni-catalyzed reductive cross-coupling has been developed to prepare enantioenriched allylic silanes. This enantioselective reductive alkenylation proceeds under mild conditions and exhibits good functional group tolerance. The chiral allylic silanes prepared here undergo a variety of stereospecific transformations, including intramolecular Hosomi–Sakurai reactions, to set vicinal stereogenic centers with excellent transfer of chirality
This dissertation describes new methods of asymmetric synthesis of diastereomeric and enantiomeric p...
Disclosed here is a catalytic strategy for asymmetric access to chiral tetrasubstituted silicon-ster...
Cross-coupling reactions have emerged as powerful methods to form carbon-carbon and carbon-heteroato...
An asymmetric Ni-catalyzed reductive cross-coupling has been developed to prepare enantioenriched a...
Over the years, the Fu group has demonstrated enantioconvergent cross-coupling reactions to be power...
Nickel-catalyzed reductive cross-coupling reactions allow for the use of bench-stable electrophiles ...
Functionalized enantiopure organosilanes are important building blocks with applications in various ...
A highly enantioselective conjugate addition of Grignard reagents to 3-silyl unsaturated esters to d...
Intramolecular Pd(0)- and Ni(0) catalyzed alkene allylations, coupled with ,&eliminations or methoxy...
Metal‐catalyzed enantioconvergent cross‐coupling reactions of alkyl electrophiles are emerging as a ...
Chiral organosilanes do not exist in nature and are therefore absent from the “chiral pool”. As a co...
In recent years, cyclic silicon-stereogenic silanes were successfully employed as stereoinducers in ...
A highly enantioselective synthesis of 3-aryl-, vinyl-, and alkynyl-2,1-benzoxasiloles (up to 99.9% ...
Catalytic enantioselective conjugate additions of organometallic reagents to electron-deficient alke...
The iron-catalyzed highly Markovnikov-type selective and enantioselective hydrosilylation of termina...
This dissertation describes new methods of asymmetric synthesis of diastereomeric and enantiomeric p...
Disclosed here is a catalytic strategy for asymmetric access to chiral tetrasubstituted silicon-ster...
Cross-coupling reactions have emerged as powerful methods to form carbon-carbon and carbon-heteroato...
An asymmetric Ni-catalyzed reductive cross-coupling has been developed to prepare enantioenriched a...
Over the years, the Fu group has demonstrated enantioconvergent cross-coupling reactions to be power...
Nickel-catalyzed reductive cross-coupling reactions allow for the use of bench-stable electrophiles ...
Functionalized enantiopure organosilanes are important building blocks with applications in various ...
A highly enantioselective conjugate addition of Grignard reagents to 3-silyl unsaturated esters to d...
Intramolecular Pd(0)- and Ni(0) catalyzed alkene allylations, coupled with ,&eliminations or methoxy...
Metal‐catalyzed enantioconvergent cross‐coupling reactions of alkyl electrophiles are emerging as a ...
Chiral organosilanes do not exist in nature and are therefore absent from the “chiral pool”. As a co...
In recent years, cyclic silicon-stereogenic silanes were successfully employed as stereoinducers in ...
A highly enantioselective synthesis of 3-aryl-, vinyl-, and alkynyl-2,1-benzoxasiloles (up to 99.9% ...
Catalytic enantioselective conjugate additions of organometallic reagents to electron-deficient alke...
The iron-catalyzed highly Markovnikov-type selective and enantioselective hydrosilylation of termina...
This dissertation describes new methods of asymmetric synthesis of diastereomeric and enantiomeric p...
Disclosed here is a catalytic strategy for asymmetric access to chiral tetrasubstituted silicon-ster...
Cross-coupling reactions have emerged as powerful methods to form carbon-carbon and carbon-heteroato...