4’-Ethyl 1,2-dimethyl 1’,5-dibenzyl-4,4-dicyano-2’-oxo-5’-phenyl-1’,2’,4a,5-tetrahydro-4H-spiro[benzo[4,5]imidazo[1,2-a]pyridine-3,3’-pyrrole]-1,2,4’-tricarboxylate
The 1,4-dipolar cycloaddition of the ylidene derivative of 1H-pyrrole-2,3-dione to a dipole generated in situ from 1-benzylbenzimidazole and dimethyl acetylenedicarboxylate proceeds via the exocyclic multiple bond of the ylidene derivative and affords a mixture of diastereomeric spiro[benzo[4,5]imidazo[1,2-a]pyridine-3,3’-pyrroles], which slowly epimerized in a solution.
Authors
- А. Н. Масливец (ORCID: https://orcid.org/0000-0001-7148-4450)
- A. A. Moroz (ORCID: https://orcid.org/0000-0003-3951-7691)
- М. В. Дмитриев (ORCID: https://orcid.org/0000-0002-8817-0543)
Institutions
- Perm State University (RU)
Publication Details
- Journal
- Molbank
- Published
- 2026-01-04
- DOI
- https://doi.org/10.3390/m2118
- Primary Topic
- Synthesis and Characterization of Pyrroles
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministry of Science and Higher Education of the Russian Federation