Once the metalloenamine intermediate is generated, it can be used as a nucleophile in an electrophilic alkylation reaction. This involves the addition of an electrophilic alkylating agent, such as an alkyl halide, to the metalloenamine.
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(1R,2'S)-(-)-N-[2'-(3,4-dimethoxyphenyl)propyl]-2-methoxy-1-phenylethylamine
6-[1,3]Dithian-2-yl-3,5,5-trimethyl-cyclohex-2-enone
