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Transfer Hydrogenation of Acyclic and Cyclic Imines

Hantzsch ester (2.2 equiv) to give p.y unsaturated a amino esters. Although the chemical yields were moderate, high enantio and trans selectivities were achieved using the same chiral phosphoric acid catalyst Ig. [Pg.112]

Cascade Transfer Hydrogenation of Quinoline and Pyridine Derivatives [Pg.113]

2 hydride addition to imines L with generation of the stereogenic center provides enantioenriched tetrahydroquinoline products. [Pg.114]

Rueping et al. further extended the method to the hydrogenation of 3 substituted [Pg.114]

Rueping and Antonchick developed an organocatalytic multiple cascade sequence [Pg.116]


See other pages where Transfer Hydrogenation of Acyclic and Cyclic Imines is mentioned: [Pg.109]   


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Acyclic imines

Cyclic hydrogen

Cyclic hydrogenation

Cyclic imine

Cyclic imines

Cyclic imines, transfer hydrogenation

Cyclic transfer

Hydrogenation cyclic imine

Hydrogenation of cyclic imines

Hydrogenation of imines

Imines cyclic, hydrogenation

Imines hydrogenation

Imines transfer

Imines transfer hydrogenation

Imines, and

Of imines

Transfer hydrogenation of cyclic imines

Transfer hydrogenation of imines

Transfer of hydrogen

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