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AZOMETHINE YLIDES DERIVED FROM ALKYL(3-OXOPIPERAZIN-2-YL)ACETATES IN 1,3-DIPOLAR CYCLOADDITION REACTIONS WITH N-ARYL MALEIMIDES

С. М. Медведева, Г. А. Сташина, С. И. Фирганг, Е. С. Маликова, М. Ю. Крысин, Х. С. Шихалиев
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Abstract


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.

How to Cite
Medvedeva, S. M.; Stashina, G. A.; Firgang, S. I.; Malikova, E. S.; Krysin, M. Yu.; Shikhaliev, Kh. S. Chem. Heterocycl. Compd. 2014, 50, 537. [Khim. Geterotsikl. Soedin. 2014, 586.]

For this article in the English edition see DOI 10.1007/s10593-014-1504-5


Keywords


alkyl(3-oxopiperazin-2-yl)acetate; N-aryl maleimide; azomethine ylide; decahydro-3bH-pyrrolo[3',4':3,4]pyrrolo[1,2-a]pyrazine; diastereomer; 1,3-dipolar cycloaddition

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