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Grignard reagents pyrrole, reactions with electrophiles

Heterocyclic aromatic compounds such as pyrrole are readily metallated with Grignard reagents. The resulting compounds have N"Mg bonds and are, therefore, not organometallic compounds, but on reaction with electrophiles give 2-substituted pyrroles [14] (eq (4)). The reaction of chloroform or bromoform with PrMgCl at -78 °C in THF-HMPA (4 1) is mild and convenient method for the generation of an unstable carbenoid in the solution [15] (eq (5)). [Pg.335]


See other pages where Grignard reagents pyrrole, reactions with electrophiles is mentioned: [Pg.59]    [Pg.79]    [Pg.320]    [Pg.59]    [Pg.79]    [Pg.224]    [Pg.308]    [Pg.413]    [Pg.161]    [Pg.59]    [Pg.79]    [Pg.224]    [Pg.308]    [Pg.420]    [Pg.461]    [Pg.385]   
See also in sourсe #XX -- [ Pg.32 , Pg.237 ]




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Electrophilic reactions Grignard reagents

Grignard reagents reactions

Grignard reagents reactions with electrophiles

Pyrrole Grignard reagents

Pyrrole reactions

Pyrroles electrophilic

Pyrroles reaction

Reaction with Grignard reagents

Reaction with pyrroles

Reactions with electrophiles

Reactions with electrophilic reagents

Reagent electrophilic

With Electrophiles

With Grignard Reagents

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