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Enolate anions, arylation effects

Seven-membered and Larger Rings. The previously mentioned photochemical substitution of an aryl halide by an enolate anion (5rn1 reaction) has been effectively utilized in the synthesis of six-, seven-, eight-, and ten-membered rings. The most notable application was to the synthesis of cephalotaxinone (116) (Scheme 37), Other workers have used photochemical dehydro-halogenation reactions to prepare related compounds. ... [Pg.346]


See other pages where Enolate anions, arylation effects is mentioned: [Pg.41]    [Pg.4]    [Pg.144]    [Pg.625]    [Pg.14]    [Pg.178]    [Pg.870]    [Pg.458]    [Pg.386]    [Pg.111]    [Pg.107]    [Pg.163]    [Pg.178]    [Pg.386]    [Pg.196]    [Pg.761]   
See also in sourсe #XX -- [ Pg.774 ]




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Anion effects

Anions anion effect

Aryl anions

Aryl effect

Arylations enolates

Enolate anions

Enolates anion

Enolates anionic

Enolates arylation

Enolization, effect

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