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Quantitative synthesis and NMR characterization of perhydro-1,3,5-tris(alkylpolyalkoxyl)-S-triazines
โ Scribed by Thomas J. Wolak; Kurt F. Wollenberg; Paul E. Adams
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2000
- Tongue
- English
- Weight
- 213 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
Abstract
Unhindered polyalkoxylated primary amines, upon treatment with an equimolar equivalent of formalde hyde, cyclized quantitatively to afford perhydroโ1,3,5โsโtriazines. This sereis of derivatives, based upon primary amine terminated poly(propylene and butylene oxides), possessed a molecular weight range of 1,900โ5,800. Structure confirmation was accomplished by gel permeation chromatography and 2D nmr spectroscopy methods.
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## Abstract 1โPhenylโ3,5โdioxopyrazolidine 1 reacts with carbon disufide and alkyl halides in presence of excess of sodium acetate in dimethylformamide to afford the ketene dithioacetals 3aโh. The ^13^C chemical shift assignments of these compounds were made on the basis of twoโdimensional nmr stud