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Aldol reactions acyl-transition metal complexes

ALDOL REACTIONS OF METAL ENOLATES OF ACYL-TRANSITION METAL COMPLEXES... [Pg.314]

Cyclic cobalt-acyl complexes can be deprotonated, and subsequent reaction of these enolates with aldehydes gives predominantly the anti/threo product (Scheme 63). Rhenium-acyl complexes can be deprotonated in the same manner. These lithium enolates can be alkylated or can react with [M(CO)5(OTf)] (M = Re, Mn) to give the corresponding enolates (Scheme Many transition metal enolates of type (21) or (22) are known, - but only a few have shown normal enolate behavior , e.g. aldol reaction, reaction with alkyl halides, etc. Particularly useful examples have been developed by Molander. In a process analogous to the Reformatsky reaction, an a-bromo ester may be reduced with Smia to provide excellent yields of condensation products (Scheme 65) which are generated through intermediacy of a samarium(III) enolate. ... [Pg.127]


See other pages where Aldol reactions acyl-transition metal complexes is mentioned: [Pg.301]    [Pg.301]    [Pg.301]    [Pg.293]    [Pg.314]    [Pg.127]    [Pg.314]    [Pg.277]    [Pg.314]    [Pg.303]   
See also in sourсe #XX -- [ Pg.2 , Pg.314 ]

See also in sourсe #XX -- [ Pg.314 ]

See also in sourсe #XX -- [ Pg.314 ]

See also in sourсe #XX -- [ Pg.2 , Pg.314 ]

See also in sourсe #XX -- [ Pg.314 ]




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Acyl metalate

Acylation Acyl complexes

Aldol reactions complexes

Aldol reactions metallated

Aldol reactions metallation

Metal complexes reactions

Transition complexes, reaction

Transition metal complexes aldol reaction

Transition metal complexes, reactions

Transition metal reactions

Transition metal-acyl complexes

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