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Allenyl enolate electrophilic trapping

As previously mentioned, allenes can only be obtained by 1,6-addition to acceptor-substituted enynes when the intermediate allenyl enolate reacts regioselectively with an electrophile at C-2 (or at the enolate oxygen atom to give an allenyl ketene acetal see Scheme 4.2). The regioselectivity of the simplest trapping reaction, the protonation, depends on the steric and electronic properties of the substrate, as well as the proton source. Whereas the allenyl enolates obtained from alkynyl enones 22 always provide conjugated dienones 23 by protonation at G-4 (possibly... [Pg.154]

Scheme 4.3. Regioselectivity of trapping reactions of acyclic allenyl enolates with different electrophiles. Scheme 4.3. Regioselectivity of trapping reactions of acyclic allenyl enolates with different electrophiles.

See other pages where Allenyl enolate electrophilic trapping is mentioned: [Pg.62]    [Pg.65]    [Pg.647]    [Pg.670]    [Pg.674]    [Pg.91]    [Pg.150]    [Pg.91]    [Pg.150]    [Pg.91]    [Pg.150]    [Pg.647]    [Pg.674]    [Pg.647]    [Pg.670]    [Pg.674]    [Pg.777]   
See also in sourсe #XX -- [ Pg.155 ]

See also in sourсe #XX -- [ Pg.155 ]




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