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Endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines
- endo-Mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined as a route to the synthesis of condensed thiazolidines. The scope of these reactions and stereochemical outcome are discussed and explained using quantum chemical calculations.
| Author details: | Milovan Stojanovic, Rade Markovic, Erich KleinpeterORCiDGND, Marija Baranac-StojanovicORCiD |
|---|---|
| DOI: | https://doi.org/10.1016/j.tet.2011.10.011 |
| ISSN: | 0040-4020 |
| Title of parent work (English): | Tetrahedron |
| Publisher: | Elsevier |
| Place of publishing: | Oxford |
| Publication type: | Article |
| Language: | English |
| Year of first publication: | 2011 |
| Publication year: | 2011 |
| Release date: | 2017/03/26 |
| Tag: | Condensed thiazolidines; Quantum chemical calculations; Vinylogous N-acyliminium ion; endo-Mode cyclization |
| Volume: | 67 |
| Issue: | 49 |
| Number of pages: | 14 |
| First page: | 9541 |
| Last Page: | 9554 |
| Funding institution: | Ministry of Science of the Republic of Serbia [142007]; Deutscher Akademischer Austauschdienst (DAAD) [504 252 70] |
| Organizational units: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie |
| Peer review: | Referiert |
