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Heterocycles, acylation metal carbenes

Generally, isocyanides can be attacked by proton bases HX (X = OR, RNH) in a nucleophilic reaction that leads to acylic heterocarbene complexes [27, 28] The use of functionalized isocyanides containing both the isocyanide group and the nucleophile in the same molecule gives access to complexes with heterocyclic carbene ligands via an 1,2-addition across the C=N triple bond [29]. A number of research groups have been active in the development of nucleophile-functionalized isocyanides, which could subsequently be cyclized in metal template-controlled reactions. [Pg.117]


See other pages where Heterocycles, acylation metal carbenes is mentioned: [Pg.4128]    [Pg.4127]    [Pg.223]    [Pg.425]    [Pg.4]    [Pg.98]    [Pg.4]    [Pg.748]    [Pg.255]    [Pg.98]    [Pg.482]    [Pg.235]   
See also in sourсe #XX -- [ Pg.1247 ]




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Acyl carbene

Acyl carbenes

Acyl metalate

Carbenes heterocyclic

Heterocycles acylation

Heterocycles metalations

Heterocycles, acylation metalation

Heterocyclic acylated

Heterocyclic carbene

Metal carbenes

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