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Organocatalysts in addition

Chiral BINOL (60) is a bifunctional organocatalyst in addition to the phenolic Brpnsted acid groups, it has a Lewis base unit attached via a spacer moiety.167 This particular combination holds the groups in a conformational lock, where they can doubly activate a substrate while giving a high level of stereocontrol. For this example of an aza-Morita-Baylis-Hillman reaction of an enone and an imine, yields up to 100% and ees up to 96% have been achieved. [Pg.22]


See other pages where Organocatalysts in addition is mentioned: [Pg.222]    [Pg.664]    [Pg.664]   
See also in sourсe #XX -- [ Pg.33 ]




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