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Cycloheptatrienes, isomerisation

The reaction of alkenylcarbene complexes and alkynes in the presence of Ni(0) leads to cycloheptatriene derivatives in a process which can be considered as a [3C+2S+2S] cycloaddition reaction [125]. As shown in Scheme 77, two molecules of the alkyne and one molecule of the carbene complex are involved in the formation of the cycloheptatriene. This reaction is supposed to proceed through the initial formation of a nickel alkenylcarbene complex. A subsequent double regioselective alkyne insertion produces a new nickel carbene complex, which evolves by an intramolecular cycloprop anation reaction to form a nor-caradiene intermediate. These species easily isomerise to the observed cycloheptatriene derivatives (Scheme 77). [Pg.110]


See other pages where Cycloheptatrienes, isomerisation is mentioned: [Pg.110]    [Pg.354]    [Pg.110]    [Pg.354]    [Pg.8]    [Pg.385]    [Pg.96]   
See also in sourсe #XX -- [ Pg.354 , Pg.355 ]

See also in sourсe #XX -- [ Pg.354 , Pg.355 ]

See also in sourсe #XX -- [ Pg.477 ]




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1.3.5- Cycloheptatrien

Cycloheptatrienes

Isomerisations

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