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The title compound, C29H33NO8, is a product of the Michael addition of the cyclic secondary amine subunit of the aza-14-crown-4 ether to dimethyl acetyl­enedicarboxyl­ate. The piperidinone ring exhibits a distorted chair conformation, and the dimethyl ethylenedicarboxylate fragment has a cis configuration with a dihedral angle of 78.96 (5)° between the two carboxyl­ate groups. The crystal packing is stabilized by weak C—H...O hydrogen bonds.

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The title compound, C25H28N2O5, is a product of the Petrenko–Kritchenko condensation of N-acetyl­piperidone with 1,5-bis­(2-formyl­phen­oxy)-3-oxapentane and ammonium acetate. The mol­ecule comprises a fused penta­cyclic system containing an aza-14-crown-3-ether macrocycle, two piperidone and two benzene rings. The aza-14-crown-3-ether ring adopts a bowl conformation. The dihedral angle between the benzene rings fused to the aza-14-crown-4-ether unit is 70.18 (4)°. The central piperidone ring has a boat conformation, whereas the terminal piperidone ring adopts a chair conformation. The conformation of the central piperidone ring is determined by two intra­molecular N—H...O hydrogen bonds. In the crystal, mol­ecules are linked by weak C—H...O inter­actions into chains along [010].

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The title compound, C31H34N2O9, is a product of the Michael addition of the cyclic secondary amine subunit of the (bis­pidino)aza-14-crown-4 ether to dimethyl acetyl­ene­dicarboxyl­ate. The mol­ecule comprises a tricyclic system containing the aza-14-crown-3 ether macrocycle and two six-membered piperidinone rings. The aza-14-crown-3-ether ring adopts a bowl conformation with a dihedral angle between the planes of the fused benzene rings of 51.14 (5)°. The central piperidone ring has a boat conformation, whereas the terminal piperidone ring adopts a chair conformation. The dimethyl ethyl­enedicarboxyl­ate fragment has a cis configuration with a dihedral angle of 56.56 (7)° between the two carboxyl­ate groups. The crystal packing is stabilized by weak C—H...O hydrogen bonds.
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