| Summary: | This thesis describes my work on nickel-catalyzed asymmetric transfer hydrogenation of unsaturated C=C and C=N bonds using various hydride sources. It contains three main parts.
Chapter one reported a highly enantioselective asymmetric hydrogenation of a,b-unsaturated esters with a chiral phosphine ligand, (R)-Me-DuPhos. With formic acid and triethyl amine worked as hydrogen source, excellent conversion and enantioselectivity were obtained. Furthermore, deuterium labeling experiments revealed a possible mechanism. I also reported asymmetric transfer hydrogenation of a,b-unsatureated esters with DMF and water as hydride source.
Chapter two described asymmetric transfer hydrogenation of cinnamates, beta- dehydroacetamidoesters and hydrazones with acetic acid and indium powder. With nickel/(S)-Binapine or (R)-Me-DuPhos catalytic system, a series of C=C and C=N gave high enantioselectivities.
Chapter three reported asymmetric deuteration of a,b-unsaturated esters with deuterium water and indium powder as hydride source. For all the substrates which we tested, excellent conversion, enantioselectivity and deuterium incorporation were obtained. This work provided a novel methodology for fine chiral deuterated products without expensive and explosive deuterium gas.
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