High-Yield Synthesis of Substituted and Unsubstituted Pyridinium Salts Containing a 4-Oxothiazolidine Moiety
- A new series of unsubstituted and substituted pyridinium salts bearing a 4-oxothiazolidinyl moiety has been prepared by an efficient rearrangement of 2-(1-bromoalkylidene)thiazolidin-4-ones. The process in based on three steps, namely carbon-bromine cleavage, bromine transfer, and substitution, each induced by pyridine or its derivatives, acting as base and reactant.
| Author details: | Marija Baranac-StojanovicORCiD, Jovanan Tatar, Erich KleinpeterORCiDGND, Rade Markovic |
|---|---|
| Publication type: | Article |
| Language: | English |
| Year of first publication: | 2008 |
| Publication year: | 2008 |
| Release date: | 2017/03/24 |
| Source: | Synthesis. - 13 (2008), S. 2117 - 2121 |
| Organizational units: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie |
