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Asymmetric organocatalysts chiral guanidines

Over the past decade, rapid growth has been achieved in organocatalytic asymmetric Diels-Alder and hetero-Diels-Alder reactions. Numerous organocatalysts such as chiral amines, guanidines, N-heterocyclic carbenes, Bronsted acids, and bifunctional catalysts have been successfully developed. The activation modes for these catalysts, such as imine-catalysis, enamine-catalysis, dienamine catalysis. [Pg.1159]

Reviews have featured recent applications of organocatalysts to asymmetric aldol reactions, including particular focus on catalysis by small molecules. The effects of introduction of a diaryl (oxy)methyl group into chiral auxiliaries, catalysts, and dopants have been discussed and applications of amidine-, isothiourea-, and guanidine-based nucleophilic catalysts for a range of reactions of carbonyl compounds have been highlighted. " ... [Pg.15]


See other pages where Asymmetric organocatalysts chiral guanidines is mentioned: [Pg.315]    [Pg.381]    [Pg.383]    [Pg.387]    [Pg.389]    [Pg.391]    [Pg.393]    [Pg.395]    [Pg.403]    [Pg.405]    [Pg.255]    [Pg.308]    [Pg.273]    [Pg.119]    [Pg.331]    [Pg.174]    [Pg.1149]    [Pg.1149]   
See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.2 , Pg.402 ]




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