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Heterocycles, acylation reduction with metals

A different type of metallation, directed by an acyl group at either the pyridine 3- or 4-position, uses a catalytic ruthenium complex and results in a reductive Heck-type substitution, as illustrated below. The mechanism involves insertion of the metal into a C-H bond. The process is non-polar and works equally well with electron-rich heterocycles, for example indole. ... [Pg.82]


See other pages where Heterocycles, acylation reduction with metals is mentioned: [Pg.159]    [Pg.174]    [Pg.289]    [Pg.289]    [Pg.981]    [Pg.230]    [Pg.981]    [Pg.295]    [Pg.35]    [Pg.96]    [Pg.273]    [Pg.44]   


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Acyl metalate

Acyl with metallates

Acyl, reduction

Heterocycles acylation

Heterocycles metalations

Heterocycles, acylation metalation

Heterocyclic acylated

Metals reduction with

Reduction heterocycles

Reductive acylation

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