The imine-ene cyclization begins with the reaction of the imine and an alkene. This step is typically catalyzed by a Lewis acid, and the alkene should be chosen to control the desired stereochemistry.
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2,2-dimethyl-1-tosyloioeridine
N'-[(S)-4-(tert-Butyl-diphenyl-silanyloxy)-6-methyl-hept-5-enoyl]-hydrazinecarboxylic acid 2,2,2-trichloro-ethyl ester
2-[3-(methylsulfanyl)propyl]phenol
(Z)-N-benzyl-2-methylene-3-methylthio-1,4-diphenyl-3-butenylamine
2-Oxazolidinone, 3-[(1Z)-2-phenyl-1-propenyl]-
