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Tebbe methylenation organometallic reagents

There are other organometallic derivatives that give Wittig-type olefination reactions, with titanium derivatives being the most commonly used. The initial addition reaction to the carbonyl gives a transient metal-ated alcohol that leads to an alkene. An example is the Tebbe reagent, which exists as a bridged methylene species (see 683), where Cp is cyclopentadienyl. 9 The aluminum species can be varied to include chloride... [Pg.679]


See other pages where Tebbe methylenation organometallic reagents is mentioned: [Pg.79]    [Pg.200]    [Pg.756]    [Pg.259]    [Pg.334]    [Pg.170]    [Pg.676]    [Pg.1079]    [Pg.321]    [Pg.277]   


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