Back to Search
Start Over
Diastereoselective cycloaddition of isatin derived azomethine ylides to 3-nitro-2(1H)-quinolones.
- Source :
-
Tetrahedron . Mar2024, Vol. 153, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- The 1,3-dipolar cycloaddition of 3-nitro-2(1 H)-quinolones with azomethine ylides derived from sarcosine or thiazolidine-4-carboxylic acid and various 1 H -indole-2,3-diones (isatins) have been investigated. The structure and stereochemistry of the formed cycloadducts were studied in detail by X-ray diffraction and NMR spectroscopy methods. [Display omitted] [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00404020
- Volume :
- 153
- Database :
- Academic Search Index
- Journal :
- Tetrahedron
- Publication Type :
- Academic Journal
- Accession number :
- 175458001
- Full Text :
- https://doi.org/10.1016/j.tet.2024.133848