In these days, asymmetric transfer hydrogenation (ATH) is a very attractive method for synthesis of enantioenriched chiral compounds, especially fine chemicals such as drugs or agrochemicals. In this review, several topics related to the asymmetric transfer hydrogenation of ketones and cyclic or acyclic imines are discussed. Initially, the reaction mechanism of the ATH of ketones and imines, mainly 3,4-dihydroisoquinoline derivates, is examined. Next, typical reaction conditions, structural effects of the catalyst and a substrate, and analytical methods used for ATH monitoring and practical applications of the ATH in the chemical industry are described
A comparison between the two most common reduction approaches for obtaining chiral amines, asymmetri...
This review contains a summary of recent developments in the transfer hydrogenation of C=N bonds, wi...
A review on catalytic asymmetric hydrogenation of C=O double bonds is presented in the first chapte...
In this review, we consider the main processes for the asymmetric transfer hydrogenation of ketones ...
Over the past few decades, Ru catalyzed transfer hydrogenation (TH) and asymmetric transfer hydrogen...
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
Derivatives of enantiomerically pure 1,2-cyclohexanediamine and 1,2- diphenylethanediamine have been...
Asymmetric hydrogen transfer (ATH) is one of the methods of stereoselective reduction of prochiral c...
In this account, we describe the design, synthesis and applications of tethered versions of the Ru(I...
In this review, we consider the main processes for the asymmetric transfer hydrogenation of ketones ...
In this research work simple unsymmetrical 1,3-diamines were studied. The synthesis of the diamines ...
Asymmetric transfer hydrogenation (ATH) is an important catalytic process in the fragrance and pharm...
A series of Ru(II)/arene complexes containing N-alkylated derivatives of TsDPEN were prepared and te...
The use of an enantiomerically pure amino alcohol, coupled to a transfer hydrogenation process, in t...
A comparison between the two most common reduction approaches for obtaining chiral amines, asymmetri...
This review contains a summary of recent developments in the transfer hydrogenation of C=N bonds, wi...
A review on catalytic asymmetric hydrogenation of C=O double bonds is presented in the first chapte...
In this review, we consider the main processes for the asymmetric transfer hydrogenation of ketones ...
Over the past few decades, Ru catalyzed transfer hydrogenation (TH) and asymmetric transfer hydrogen...
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
Derivatives of enantiomerically pure 1,2-cyclohexanediamine and 1,2- diphenylethanediamine have been...
Asymmetric hydrogen transfer (ATH) is one of the methods of stereoselective reduction of prochiral c...
In this account, we describe the design, synthesis and applications of tethered versions of the Ru(I...
In this review, we consider the main processes for the asymmetric transfer hydrogenation of ketones ...
In this research work simple unsymmetrical 1,3-diamines were studied. The synthesis of the diamines ...
Asymmetric transfer hydrogenation (ATH) is an important catalytic process in the fragrance and pharm...
A series of Ru(II)/arene complexes containing N-alkylated derivatives of TsDPEN were prepared and te...
The use of an enantiomerically pure amino alcohol, coupled to a transfer hydrogenation process, in t...
A comparison between the two most common reduction approaches for obtaining chiral amines, asymmetri...
This review contains a summary of recent developments in the transfer hydrogenation of C=N bonds, wi...
A review on catalytic asymmetric hydrogenation of C=O double bonds is presented in the first chapte...