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Phosphorus-carbon bonds nitrogen halides

In intramolecular arylations, a new bond is created between two aromatic moieties of the same molecule or between an aromatic nucleus and an atom of a side-chain. Many intramolecular arylation reactions of homocyclic and heterocyclic aromatic halides have been studied mainly in view of their synthetic applications, and it is not always clear which mechanistic pathway is followed. The reaction may start with homolytic or heterolytic dissociation of the carbon-halogen bond and proceed by attack of the aryl radical or aryl cation on another part of the molecule. Electrocyclization followed by elimination of hydrogen halide is another possibility. Especially when heteroatoms such as nitrogen, sulphur or phosphorus are involved, the initial step may be a nucleophilic attack on the carbon atom bearing the halide atom. [Pg.924]

Acid anhydrides Carbon-carbon bonds Halide bonds Phosphorus-nitrogen Sulfur-nitrogen bonds... [Pg.1107]


See other pages where Phosphorus-carbon bonds nitrogen halides is mentioned: [Pg.2808]    [Pg.636]    [Pg.2807]    [Pg.374]    [Pg.3006]    [Pg.338]    [Pg.170]    [Pg.146]    [Pg.913]    [Pg.26]    [Pg.3753]    [Pg.3752]    [Pg.898]    [Pg.552]    [Pg.23]    [Pg.811]    [Pg.839]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.7 ]




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Bond carbon-nitrogen

Bond carbon-phosphorus

Carbon halides

Carbon-phosphorus

Halide bond

Nitrogen carbon—phosphorus bonds

Nitrogen halides

Nitrogen phosphorus halides

Nitrogen—phosphorus bonds

Phosphorus bonding

Phosphorus carbon halides

Phosphorus halides

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