AZOMETHINE YLIDES DERIVED FROM ALKYL(3-OXOPIPERAZIN-2-YL)ACETATES IN 1,3-DIPOLAR CYCLOADDITION REACTIONS WITH N-ARYL MALEIMIDES
DOI:
https://doi.org/10.1007/1621Keywords:
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 cycloadditionAbstract
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