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Organocuprates, reaction with conjugated esters

There is also a correlation between the reduction potential of the carbonyl compound and the ease of reaction with cuprate reagents. The more easily reduced, the more reactive is the compound toward organocuprate reagents. Compounds such as a,/3-unsaturated esters and nitriles which are not as easily reduced as a,j3-unsaturated ketones do not react readily with simple alkyl cuprates even though they are good acceptors in conjugate addition reactions involving other types of nucleophiles (Michael reactions). [Pg.277]


See other pages where Organocuprates, reaction with conjugated esters is mentioned: [Pg.61]    [Pg.179]    [Pg.184]    [Pg.61]    [Pg.476]    [Pg.1049]    [Pg.462]    [Pg.323]    [Pg.76]    [Pg.1217]    [Pg.224]    [Pg.11]    [Pg.149]    [Pg.230]    [Pg.104]    [Pg.430]    [Pg.11]    [Pg.430]    [Pg.593]    [Pg.430]    [Pg.67]   
See also in sourсe #XX -- [ Pg.1027 ]

See also in sourсe #XX -- [ Pg.650 ]




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Conjugate reaction

Conjugated reaction

Conjugative reactions

Esters, conjugated

Organocuprate

Organocuprates

Reaction with conjugated esters

Reaction with organocuprates

With organocuprates

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