Reductive cyclization typically involves the formation of a cyclic compound with the concurrent reduction of a functional group. This reduction may involve the addition of hydrogen atoms.
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2-iodo-5-methoxybenzophenone
cis-3-Ethyl-3-chloropropyl-4a-(nitroethyl)-9-benzylhexahydrocarbazol-4-one
1-(2’-nitrophenyl)-3,4-dihydronaphthalene
(1SR,2RS)-α-benzylcyclopentanol
(+/-)-(4R,5R)-2-amino-1,3,3-tricyano-4,5-diphenylcyclopentene
3-[(3-phenyl)-2-oxo-2H-quinoxalin-1-yl]propionic acid ethyl ester
