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   <subfield code="a">L-proline-catalysed synthesis of functionalized unsymmetrical dihydro-1H-indeno[1,2-b]pyridines</subfield>
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   <subfield code="a">Aromatic aldehydes have been employed in a one-pot four-component reaction with ethyl acetoacetate, 1,3-indandione and ammonium acetate in the presence of L-proline in water and under reflux condition to afford the corresponding dihydro-1H-indeno[1,2-b]pyridines in very good yields. Graphical Abstract Aromatic aldehydes have been employed in a one-pot four component reaction with ethyl acetoacetate, 1,3-indanedione and ammonium acetate in the presence of L-proline in water and under reflux condition to afford the corresponding dihydro-1H-indeno[1, 2-b]pyridines in good yields.</subfield>
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