“…51 The treatment of three equivalents of malononitrile with 3-methylcyclohex-2-enone (82) The reaction of quinoxalinium salt 91 with two equivalents of malononitrile produced 2-iminocyclopentaquinoxalines 92 (Scheme 21). 55 The literature data presented above demonstrates that many multicomponent reactions utilize malononitrile as a characteristic reagent in carbocyclic synthesis with valuable synthetic potential.…”
“…51 The treatment of three equivalents of malononitrile with 3-methylcyclohex-2-enone (82) The reaction of quinoxalinium salt 91 with two equivalents of malononitrile produced 2-iminocyclopentaquinoxalines 92 (Scheme 21). 55 The literature data presented above demonstrates that many multicomponent reactions utilize malononitrile as a characteristic reagent in carbocyclic synthesis with valuable synthetic potential.…”
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