Abstract
A highly efficient one-pot synthesis of some new spiro-2-aminopyrimidinones via a three-component reaction of cyclic ketones, methylcyanoacetate or malononitrile, and guanidinium carbonate has been developed through a domino Knoevenagel/Michael/cyclization sequence. The hydrogen bonding capacity of these compounds would make these structures especially stable. Furthermore, the antibacterial study reveals that these types of compounds exhibit good antibacterial activity.
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