Abstract:A remarkably efficient double crossed aldol condensation of piperidin-4-one with various aromatic aldehydes is described at room temperature in the presence of diethylamine and lithium perchlorate under solvent-free conditions. Excellent yields of 3,5-bis(arylmethylidene)piperidinones are achieved in a facile one-pot general procedure. Structure of the products is determined by spectroscopic methods and elemental analysis.
Synthesis of Bis(arylmethylidene)piperidinones -[by a remarkably efficient double crossed aldol condensation of piperidinone with various aromatic aldehydes]. -(ABAEE*, M. S.; MOJTAHEDI, M. M.; SHARIFI, R.; ZAHEDI, M. M.; J.
Synthesis of Bis(arylmethylidene)piperidinones -[by a remarkably efficient double crossed aldol condensation of piperidinone with various aromatic aldehydes]. -(ABAEE*, M. S.; MOJTAHEDI, M. M.; SHARIFI, R.; ZAHEDI, M. M.; J.
The one‐pot, three‐component Mannich reactions of thiopyran‐4‐one 1 with different aromatic aldehydes and aniline derivatives in the presence of catalytic quantities of ZrOCl2.8H2O (15 mol %) led to rapid and high yield formation of various 3‐methylamino substituted derivatives of 1 at room temperature. Spectroscopic and X‐ray analyses of the products suggested the formation of the anti stereoisomers as the major product of the reactions.
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