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ChemInform Abstract: A Convenient Synthesis of New Biological Active 5‐Imino‐4‐thioxo‐2‐imidazolidinones Involving Acetonitrile Electrogenerated Base. Issue 4 (January 2016)
Record Type:
Journal Article
Title:
ChemInform Abstract: A Convenient Synthesis of New Biological Active 5‐Imino‐4‐thioxo‐2‐imidazolidinones Involving Acetonitrile Electrogenerated Base. Issue 4 (January 2016)
Main Title:
ChemInform Abstract: A Convenient Synthesis of New Biological Active 5‐Imino‐4‐thioxo‐2‐imidazolidinones Involving Acetonitrile Electrogenerated Base.
Abstract: Acetonitrile is electrolyzed to form cyanomethyl anion, which not only deprotonizes benzyl amines [e.g. (I)] to give a nitride intermediate, but also forms an organomagnesium compound with the magnesium anode.