Various combinations of chiral ligands and transition metal sources have been used as catalysts in the enantioselective alkynylation of aldehydes and ketones. The results of previous studies and current investigations are reviewed. The factors governing the yields and enantioselectivities are discussed.Department of Applied Biology and Chemical Technolog
The new readily available sulfamide-amine alcohol 11 was found to be effective in catalyzing enantio...
The catalytic asymmetric addition of alkyl groups to aldehydes is an important reaction in the enant...
The smooth addition of phenylacetylene to aromatic ketones in the presence of catalytic amounts of C...
Asymmetric alkynylation of ketones can provide versatile chiral tertiary propargylic alcohols. A ser...
A series of amino alcohol ligands of binaphthyl derivatives were synthesized and were found to be ef...
xiii, 185 leaves : ill. ; 30 cm.PolyU Library Call No.: [THS] LG51 .H577P ABCT 2003 LuChiral proparg...
A series of sulfonamides (2-4) were prepared from natural amino acids and used as additives in the B...
The present article describes the recent catalytic asymmetric methods developed in our group to acce...
A simple and practical method to make chiral propargylic alcohols has been developed: in the presenc...
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
Applications of chiral aluminum catalysts to asymmetric Diels-Alder reaction, Michael addition react...
Controlling the absolute stereochemistry of molecules is a major challenge to contemporary chemists....
The present article describes the recent catalytic asymmetric methods developed in our group to acce...
The application of the same metallic chiral binuclear complexes containing rhodium, palladium, titan...
The enantioselective catalytic alkynylation of aromatic aldehydes is reported using a sterically hig...
The new readily available sulfamide-amine alcohol 11 was found to be effective in catalyzing enantio...
The catalytic asymmetric addition of alkyl groups to aldehydes is an important reaction in the enant...
The smooth addition of phenylacetylene to aromatic ketones in the presence of catalytic amounts of C...
Asymmetric alkynylation of ketones can provide versatile chiral tertiary propargylic alcohols. A ser...
A series of amino alcohol ligands of binaphthyl derivatives were synthesized and were found to be ef...
xiii, 185 leaves : ill. ; 30 cm.PolyU Library Call No.: [THS] LG51 .H577P ABCT 2003 LuChiral proparg...
A series of sulfonamides (2-4) were prepared from natural amino acids and used as additives in the B...
The present article describes the recent catalytic asymmetric methods developed in our group to acce...
A simple and practical method to make chiral propargylic alcohols has been developed: in the presenc...
The catalytic asymmetric synthesis of tertiary alcohols by the addition of organometallic reagents t...
Applications of chiral aluminum catalysts to asymmetric Diels-Alder reaction, Michael addition react...
Controlling the absolute stereochemistry of molecules is a major challenge to contemporary chemists....
The present article describes the recent catalytic asymmetric methods developed in our group to acce...
The application of the same metallic chiral binuclear complexes containing rhodium, palladium, titan...
The enantioselective catalytic alkynylation of aromatic aldehydes is reported using a sterically hig...
The new readily available sulfamide-amine alcohol 11 was found to be effective in catalyzing enantio...
The catalytic asymmetric addition of alkyl groups to aldehydes is an important reaction in the enant...
The smooth addition of phenylacetylene to aromatic ketones in the presence of catalytic amounts of C...