2′-Methyl-2′-nitro-1′-phenyl-2′,3′,5′,6′,7′,7a'-hexahydrospiro[indoline-3,3′-1′H-pyrrolizin]-2-one
Autor: | Yaghoub Sarrafi, Kamal Alimohammadi |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2008 |
Předmět: | |
Zdroj: | Acta Crystallographica Section E, Vol 64, Iss 8, Pp o1490-o1490 (2008) |
Druh dokumentu: | article |
ISSN: | 16005368 1600-5368 |
DOI: | 10.1107/S1600536808020837 |
Popis: | The title compound, C21H21N3O3, was synthesized by a multi-component 1,3-dipolar cycloaddition of azomethine ylide, derived from isatin and proline by a decarboxylative route, and (E)-1-phenyl-2-nitropropene. In the molecule, the spiro junction links a planar oxindole ring and a pyrrolidine ring in an envelope conformation. The molecular packing is stabilized by an intermolecular N—H...N interaction of the oxindole and pyrrolizidine rings. |
Databáze: | Directory of Open Access Journals |
Externí odkaz: |