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Elcb Eliminations in protecting group chemistry

It was indicated already in Section 4.1.5 that Het /HeE-eliminations offer possibilities for regio- and stereocontrol in the synthesis of alkenes that are quite different from those of H/Het-eliminations. It was also indicated that the value of these reactions for alkene synthesis depends on, among other things, how laborious it is to obtain the Het -and Het2-contain-ing substrates. Accordingly, in the next sections we will discuss such eliminations and the preparation of the elimination precursors as well. [Pg.194]

A /1-elimination of this type—often also referred to as fragmentation—takes place in the initiation of a Grignard reaction using ethylene bromide  [Pg.194]

The purpose of this operation is not to release ethylene but to etch the Mg shavings. [Pg.194]

A second example of this type of elimination is the generation of dichloroketene from trichloroacetyl chloride and zinc  [Pg.195]

You should remember that fi-heterosubstituted saturated organometallic compounds hardly ever exist. On the contrary, they generally fragment through M /Het -elimination to an alkene  [Pg.195]


See other pages where Elcb Eliminations in protecting group chemistry is mentioned: [Pg.192]    [Pg.158]   
See also in sourсe #XX -- [ Pg.158 ]




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