平成13年度機能研所長リーダーシップ経費(若手奨励研究)による研究の紹介This research project aims to develop a new and effective catalytic asymmetric synthesis on the basis of an activation method using a chiral Lewis acid catalyst. From this viewpoint, an effective asymmetric conjugate addition reaction of electron-rich aromatic compounds to sulfonyl-functionalized enones is examined in the presence of chiral Lewis acids. Furthermore, the synthesis of a variety of optically active derivatives is also performed by the transformation of the β-keto sulfone moiety of conjugated adducts
THESIS 8462The research carried out in the present study focuses mainly on the synthesis of some nov...
The concept of the electron pair bond formulated by G. N. Lewis provides the foundation for our unde...
Catalysis by chiral frustrated Lewis pairs (FLPs) is almost restricted to the reduction of unsaturat...
Catalytic asymmetric conjugate addition reactions represent a powerful strategy to access chiral mol...
This account summarizes the activities of the first three years of our young research group working ...
The stereochemical stability of bromonium and chloronium ions has been investigated in the context o...
The conjugateadditionreaction is a fundamental process in organic chemistry. The reaction involves t...
The concept of Lewis base activation of Lewis acid has been successfully applied to the enantioselec...
This thesis is presented in two parts. Part 1. Asymmetric Synthesis via Chiral Sulfoximines. Chapter...
The first effective example of asymmetric conjugate addition–protonation reactions of thiols to α-su...
Electrophilic sulfur- and selenium-promoted additions of nu-cleophiles to unactivated olefins repres...
ABSTRACT: A catalytic, enantioselective, Lewis base-catalyzed α-sulfenylation of silyl enol ethers h...
Asymmetric synthesis is most significant method to generate chiral compounds from prochiral substrat...
The Lewis base activation of Lewis acids has been harnessed in the development of an enantioselectiv...
This thesis details the use of chiral diamine derived catalysts in asymmetric addition reactions. Th...
THESIS 8462The research carried out in the present study focuses mainly on the synthesis of some nov...
The concept of the electron pair bond formulated by G. N. Lewis provides the foundation for our unde...
Catalysis by chiral frustrated Lewis pairs (FLPs) is almost restricted to the reduction of unsaturat...
Catalytic asymmetric conjugate addition reactions represent a powerful strategy to access chiral mol...
This account summarizes the activities of the first three years of our young research group working ...
The stereochemical stability of bromonium and chloronium ions has been investigated in the context o...
The conjugateadditionreaction is a fundamental process in organic chemistry. The reaction involves t...
The concept of Lewis base activation of Lewis acid has been successfully applied to the enantioselec...
This thesis is presented in two parts. Part 1. Asymmetric Synthesis via Chiral Sulfoximines. Chapter...
The first effective example of asymmetric conjugate addition–protonation reactions of thiols to α-su...
Electrophilic sulfur- and selenium-promoted additions of nu-cleophiles to unactivated olefins repres...
ABSTRACT: A catalytic, enantioselective, Lewis base-catalyzed α-sulfenylation of silyl enol ethers h...
Asymmetric synthesis is most significant method to generate chiral compounds from prochiral substrat...
The Lewis base activation of Lewis acids has been harnessed in the development of an enantioselectiv...
This thesis details the use of chiral diamine derived catalysts in asymmetric addition reactions. Th...
THESIS 8462The research carried out in the present study focuses mainly on the synthesis of some nov...
The concept of the electron pair bond formulated by G. N. Lewis provides the foundation for our unde...
Catalysis by chiral frustrated Lewis pairs (FLPs) is almost restricted to the reduction of unsaturat...