Synthesis of Spiro[indole-3,2′-pyrrole]triones by the Reaction of Pyrrolobenzoxazepinetriones with Enaminoketone
The reaction of 3-aroylpyrrolo[1,2-a][4,1]benzoxazepin-1,2,4-triones with 3-cyclohexylamino-5,5-dimethylcyclohex-2-en-1-one leads to the formation of 3′-(4-aroyl)-4′-hydroxy-1′-(2-(hydroxymethyl)phenyl)-6,6-dimethyl-1-cyclohexyl-6,7-dihydrospiro[indole-3,2′-pyrrole]-2,4,5′(1H,1′H,5H)-triones. A new scheme for the interaction of 3-aroylpyrrolo[1,2-а][4,1]benzoxazepine-1,2,4-triones with N-substituted enaminoketones leading to the formation of derivatives of the difficult-to-reach heterocyclic systems of spiro[indole-3,2′-pyrrole]triones is described.
Authors
- А. Н. Масливец (ORCID: https://orcid.org/0000-0001-7148-4450)
- Anna A. Maslivetc (ORCID: https://orcid.org/0000-0003-0555-0231)
- М. В. Дмитриев (ORCID: https://orcid.org/0000-0002-8817-0543)
Institutions
- Perm State University (RU)
Publication Details
- Journal
- Журнал органической химии
- Published
- 2024-12-27
- DOI
- https://doi.org/10.31857/s0514749224020033
- Primary Topic
- Chemical synthesis and pharmacological studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00