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Azomethine Ylides Derived from Alkyl- (3-Oxopiperazin-2-yl)Acetates in 1,3-Dipolar Cycloaddition Reactions with n-Aryl Maleimides

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Chemistry of Heterocyclic Compounds Aims and scope

A 1,3-dipolar cycloaddition reaction of N-aryl maleimides with azomethine ylides obtained from aromatic aldehydes and alkyl(3-oxopiperazin-2-yl)acetates gave a new heterocyclic system – decahydro-3bH-pyrrolo[3',4':3,4]pyrrolo[1,2-a]pyrazine.

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Correspondence to Kh. S. Shikhaliev.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 586-592, April, 2014.

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Medvedeva, S.M., Stashina, G.A., Firgang, S.I. et al. Azomethine Ylides Derived from Alkyl- (3-Oxopiperazin-2-yl)Acetates in 1,3-Dipolar Cycloaddition Reactions with n-Aryl Maleimides. Chem Heterocycl Comp 50, 537–543 (2014). https://doi.org/10.1007/s10593-014-1504-5

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