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Amine alkanone imine

Initial imine or iminium generation from amines can be used to allow C-X (X = heteroatom) or C-C bond formation. Thus, anilines substituted in the orf/zo-position with X-H functionalities (X = 0, NMe, S) have been dehy-drogenatively condensed with benzylamines under mpg-CN photocatalysis to yield the corresponding benzofused heterocycles [122]. Via iminium intermediates, AI-aryl-l,2,3,4-tetrahydroisoquinolines could be dehydrogenatively coupled photocatalytically by mpg-CN to various carbon nucleophiles derived from nitroalkanes, malonates, and 2-alkanones, and the latter via tandem organocatalysis with proline [124]. [Pg.282]


See other pages where Amine alkanone imine is mentioned: [Pg.2217]    [Pg.2218]    [Pg.2543]    [Pg.2216]    [Pg.2217]    [Pg.2218]    [Pg.2543]    [Pg.1130]    [Pg.1131]    [Pg.2426]    [Pg.2435]   
See also in sourсe #XX -- [ Pg.835 , Pg.836 , Pg.837 , Pg.838 , Pg.847 , Pg.848 , Pg.849 , Pg.850 ]




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