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Substitution at carbon by organomagnesium compounds

They also reported transition metal-catalyzed regioselective substitution reac- [Pg.79]

For example, reaction of n-decyl bromide with -butylmagnesium chloride [Pg.80]

The most generally applicable catalysts are diphosphine complexes of nickel(ll) halides, notably dichloro[l,3-bis(diphenylphosphino)propane]nickel(II), NiCl2 (dppp) , and to a lesser extent analogous palladium(ll) complexes. Many examples are listed in reviews [42-44], [Pg.82]


See other pages where Substitution at carbon by organomagnesium compounds is mentioned: [Pg.152]    [Pg.154]    [Pg.156]    [Pg.158]    [Pg.160]    [Pg.162]    [Pg.164]    [Pg.166]    [Pg.168]    [Pg.170]    [Pg.172]    [Pg.174]    [Pg.176]    [Pg.178]    [Pg.180]    [Pg.253]    [Pg.154]    [Pg.156]    [Pg.158]    [Pg.160]    [Pg.162]    [Pg.164]    [Pg.166]    [Pg.168]    [Pg.170]    [Pg.172]    [Pg.174]    [Pg.176]    [Pg.178]    [Pg.180]    [Pg.76]   


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At carbon

Carbon organomagnesiums

Organomagnesium

Organomagnesium compounds

Substituted Compounds

Substitution at

Substitution at carbon

Substitution by Carbon

Substitution compounds

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