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Asymmetric Conjugate Additions of Cyanide

Lanthanide Bimetallic and Polymetallic Asymmetric Catalysts 687 Table 13.32 Catalytic asymmetric conjugate addition of cyanide to a,p-unsaturated imides (S,S)-[(salen)AI]20 (2 mol%)... [Pg.159]

Scheme 13.34 Catalytic asymmetric conjugate addition of cyanide to p-aryl, alkyl, and alkenyl ap-unsaturated /V-acyl pyrroles. Scheme 13.34 Catalytic asymmetric conjugate addition of cyanide to p-aryl, alkyl, and alkenyl ap-unsaturated /V-acyl pyrroles.
Thus, the asymmetric catalysis of cyanoethoxycarbonylation, cyanophosphoryla-tion, epoxidation of electron-deficient olefins, Michael reactions of malonates and (3-keto-esters, Strecker reaction of keto-imines, conjugate addition of cyanide to a, (3-unsaturated pyrrole amides, ring opening of meso aziridines with TMSCN and cyanosilylation of ketones (example shown below) have been successfully carried out using these complexes as asymmetric catalysts. [Pg.528]


See other pages where Asymmetric Conjugate Additions of Cyanide is mentioned: [Pg.158]    [Pg.158]    [Pg.432]    [Pg.158]    [Pg.158]    [Pg.432]    [Pg.390]    [Pg.1063]    [Pg.13]    [Pg.24]    [Pg.316]    [Pg.316]    [Pg.278]    [Pg.417]    [Pg.350]    [Pg.26]    [Pg.1377]    [Pg.318]    [Pg.318]    [Pg.110]   


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Addition asymmetric conjugated

Asymmetric addition

Asymmetric conjugate addition

Asymmetric cyanide addition

Conjugate addition cyanide

Conjugate addition of cyanide

Cyanide, conjugation

Cyanides, addition

Of cyanide

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