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Iminium catalysis

Iminium Catalysis. Together with enamine catalysis, iminium catalysis is the most prominent activation mode in asymmetric aminocatalysis [61]. Initial work was carried out on cycloadditions [10, 62], but it was rapidly extended to... [Pg.30]

Comparing the activation mode of iminium and enamine catalysis, iminium catalysis is based on a LUMO-activation mode of the electrophile whereas enamine catalysis is based on a HOMO-activation of the nucleophile. Keeping in mind the fact that enamine and iminium species are rapidly interconverted via a two-electron redox process (proton abstraction of an iminium species results in an enamine), MacMillan and co-workers reasoned that it should be possible to interrupt this equilibrium chemically by carrying out just a one-electron oxidation of an enamine. This would then generate a three-7i-electron radical cation with a singly occupied molecular orbital (SOMO) that should be activated towards catalytic transfomiatirHis (racemic or asymmetric) not possible using classical enamine or iminium activation (Scheme 80) 316). [Pg.81]


See other pages where Iminium catalysis is mentioned: [Pg.36]    [Pg.944]    [Pg.1294]    [Pg.1363]    [Pg.944]    [Pg.1294]    [Pg.1363]   
See also in sourсe #XX -- [ Pg.321 ]

See also in sourсe #XX -- [ Pg.46 ]

See also in sourсe #XX -- [ Pg.1363 ]




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