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Metallacyclobutane, 2-methylene cycloaddition reactions

Tebbe found that titanocene complexes promoted olefin metathesis in addition to carbonyl olefination. Despite the fact that these complexes have low activity, they proved to be excellent model systems. For example, the Tebbe complex exchanges methylene units with a labeled terminal methylene at a slow rate that can be easily monitored (Eq. 4.6) [54]. This exchange is the essential transformation of olefin metathesis. When reactions with olefins are performed in the presence of a Lewis base, the intermediate titanium metallacycle can be isolated and even structurally characterized (Eq. 4.7) [61] These derivatives were not only the first metathesis-active metallacyclobutane complexes ever isolated, but they were also the first metallacyclobutanes isolated from the cycloaddition of a metal-carbene complex with an olefin. These metallacycles participate in all the reactions expected of olefin metathesis catalysts, especially exchange with olefins... [Pg.203]


See other pages where Metallacyclobutane, 2-methylene cycloaddition reactions is mentioned: [Pg.1107]    [Pg.568]    [Pg.1107]   
See also in sourсe #XX -- [ Pg.293 ]

See also in sourсe #XX -- [ Pg.5 , Pg.293 ]

See also in sourсe #XX -- [ Pg.293 ]

See also in sourсe #XX -- [ Pg.5 , Pg.293 ]




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