The final step involves trapping the reactive intermediate, often through reaction with another chemical species or functional group. The trapping step can be designed to occur selectively, favoring the formation of a particular enantiomer.
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N-(phenylmethoxy)-N-2-propen-1-yl-2-propenamide
4-(1-methyl-1-phenylethyl)-quinaldine
1-(5-O-(MMTr)-2'-deoxy-2'-C,3'-O-((1-isopropyl)ethylene)-β-D-lyxofuranosyl)uracil
Trisilane, 1,1,1,3,3,3-hexamethyl-2-[4-(trifluoromethyl)benzoyl]-2-(trimethylsilyl)-
2-(Tributyl-λ5-phosphanylidene)-cyclohexane-1,3-dione
1-bromo-2-(2-phenylethyl)cycloprop-1-ene
