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Synthesis of 3,4-dihydropyrimidin-2(1H)-one via Retro-Biginelli reaction
Authors:Sudipta Mondal  Mohabul A. Mondal
Affiliation:Department of Chemistry, Jadavpur University, Kolkata, India
Abstract:Hydrolytic behavior of 5-acetyl-6-methyl-4-phenyl-3,4-dihydropyrimidin-2(1H)-one under alkaline condition has been explored. Mechanistic details are established by LCMS and HPLC. Evidence suggested that the deacetylative benzylidenation proceeds through the retro-Biginelli reaction. The scope of the retro-Biginelli reaction has been explored by the synthesis of substituted DHPs.
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