The carbanion generated in the previous step undergoes a series of intramolecular reactions. These reactions can include cyclization, rearrangement, and the formation of new carbon-carbon bonds. The precise sequence of these reactions depends on the structure of the precursor molecule.
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3-methyl-1-phenyl-9H-xanthen-9-one
4-phenyl-<2.2>paracyclophane
(2R,3S,4R)-tribenzyloxy-octa-5(E,Z),7-diene-1-al diethyl dithioacetal
(1S,5S)-6-Benzyl-4-vinylidene-6-aza-bicyclo[3.2.1]octan-7-one
cyclo<-D-Val-Orn(Z)-Leu-Phe-Pro>2
N-(Ethoxy-phenyl-methyl)-N-((E)-5-trimethylsilanyl-pent-3-enyl)-acetamide
