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Carbalumination intramolecular

Intramolecular carbaluminations of olefins are facile (in the absence of ether) and show synthetic potential . This combines monohydroalumination (see 5.3.3.4.1) of nonconjugated polyenes and carbalumination leading to the synthesis of various mono- ... [Pg.222]

Intramolecular carbalumination of alkynes is observed with the dimeric diphenyl-(phenylethynyl)aluminum. The structures of such compounds are in accord with the assumption of intermediate n-complex formation between the C=C bond and Al. Carbalumination is followed by exchange, electrophilic attack at the C=C bond and a... [Pg.225]

See other pages where Carbalumination intramolecular is mentioned: [Pg.636]    [Pg.642]    [Pg.556]    [Pg.644]    [Pg.106]   
See also in sourсe #XX -- [ Pg.758 ]

See also in sourсe #XX -- [ Pg.8 , Pg.758 ]

See also in sourсe #XX -- [ Pg.5 , Pg.10 , Pg.533 ]

See also in sourсe #XX -- [ Pg.3 , Pg.3 , Pg.5 , Pg.5 ]

See also in sourсe #XX -- [ Pg.8 , Pg.758 ]



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Carbalumination

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