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Reactions of Nucleophiles with sp2 Hybridised Carbon Centres

3 Reactions of Nucleophiles with sp2 Hybridised Carbon Centres [Pg.72]

In the same way that we were primarily concerned with reactions of nitriles in the previous section, we will be concerned with the attack of nucleophiles on imines in this section. Imines, R2C=NR, are the nitrogen analogues of carbonyl groups, and we saw in Chapter 2 that imines may be stabilised by co-ordination to a metal ion capable of back-donation to the ligand -levels. We shall investigate the synthetic utility associated with the formation of co-ordinated imines in a later chapter. However, it is also possible to promote the hydrolysis of the imine by co-ordination to a positively charged metal ion. [Pg.72]


See other pages where Reactions of Nucleophiles with sp2 Hybridised Carbon Centres is mentioned: [Pg.64]    [Pg.345]   


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Carbon centres

Carbon hybridisation

Carbon nucleophile

Carbon nucleophiles

Carbon reaction with nucleophile

Carbon with nucleophiles

Carbon-centred

Carbonate reactions with

Centre of Reactions

Hybridisation

Nucleophilic of carbonates

Reaction centre

Reaction with carbon

Reaction with nucleophiles

Reactions of Carbon Nucleophiles

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