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Carbonyl conjugate asymmetric arylation

Conjugate Asymmetric Arylation of 3-Substituted a,P-unsaturated Carbonyl Compounds... [Pg.291]

Asymmetric cyclopropanation. Optically active cyclopropanes can be prepared in optical yields as high as by reaction of certain olefins with various dia/o compounds in the presence of this catalyst. Chemical yields are usually 90 95%. However, the reaction is generally limited to terminal double bonds conjugated with an aryl or carbonyl group or with another double bond. The (1 S)-enantiomer is always obtained in large excess. [Pg.25]

See other pages where Carbonyl conjugate asymmetric arylation is mentioned: [Pg.155]    [Pg.322]    [Pg.98]    [Pg.144]    [Pg.109]    [Pg.193]    [Pg.3221]    [Pg.1319]    [Pg.286]    [Pg.590]    [Pg.98]    [Pg.3220]    [Pg.17]    [Pg.178]    [Pg.1305]    [Pg.243]    [Pg.59]    [Pg.77]    [Pg.344]    [Pg.102]   
See also in sourсe #XX -- [ Pg.271 , Pg.281 , Pg.282 , Pg.283 , Pg.283 , Pg.284 , Pg.285 , Pg.286 , Pg.287 , Pg.288 , Pg.289 , Pg.290 , Pg.291 , Pg.292 ]



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Aryl carbonylation

Asymmetric arylation

Carbonylation asymmetric

Conjugate arylation

Conjugated carbonyls

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