## Gas-phase eliminations of 4-substituted-2-alkoxythiazoline-5-ones have been studied. These compounds eliminate via a six-membered transition state to produce 4-substituted-thiazolidine-2,5-diones. These eliminations are unimolecular first-order reactions. Utilization of this thermolysis reaction
Gas-phase pyrolysis in heterocyclic synthesis. Gas-phase elimination reactions of some substituted aminoazoles
โ Scribed by Nouria A. Al-Awadi; Mohamed H. Elnagdi
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 183 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
โฆ Synopsis
Gas-phase pyrolyses of ethyl N-(5-cyanomethyl-1,3,4thiadiazol-3-yl)carbamate ( ), 1-benzoyl-3-(3-methylpyrazol-5-yl)thiourea ( ), 1-benzoyl-3-(5-methylisoxazol-3-yl)thiourea ( ), and 1-acetyl-3-(3-phenylpyrazol-5-yl)thiourea ( ) have been studied. These reactions were homogeneous and unimolecular. The kinetics obeyed the first-order rate equation. Utilization of this pyrolytic reaction in heterocyclic synthesis is considered, and mechanistic information has been obtained from kinetic data and product analysis using an on-line pyrolysis GC-MS technique. The physical constants of four new substituted aminoazoles are also described.
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Rates, Arrhenius parameters, and Hammett substituent constants are obtained for the gas-phase thermal elimination of ethyl benzoate (1) and ethyl 2 -thienyl -(2), 3thienyl -(3), 2 -furyl -(4), 3 -furyl -(5), 4 -pyridyl -(6), 3 -pyridyl -(7), and 2pyridylcarboxylate (8) esters. The log A/s ฯช1 and the
## Abstract The complete manuscript of this communication appears in: __Angew. Chem. Suppl. 1982__, 1515. DOI:10.1002/anie.198215150
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