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 |
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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 |