Event submissions
Published
This submission belongs to the session a. General Organic Synthesis of the event The 12th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2008
Citation
Maria Luisa Testa, Elena Zaballos-Garcia, Ramón J. Zaragozá, Solvent-mediated reactivity of b-aminoalcohols against dialkyloxalate: synthesis of tetrasubstituted oxalamide and/ or morpholin-2,3-dione derivatives., in Proceedings of The 12th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2008, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-12-01198
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Solvent-mediated reactivity of b-aminoalcohols against dialkyloxalate: synthesis of tetrasubstituted oxalamide and/ or morpholin-2,3-dione derivatives.
Maria Luisa Testa 1
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Elena Zaballos-Garcia 2
Ramón J. Zaragozá 3
1. Istituto per lo Studio dei Materiali Nanostrutturati, CNR, via Ugo La Malfa 153, 90146 Palermo, Italy
2. Departamento Química Orgánica, Universidad de Valencia, Av. Vicente Andres Estelles, E- 46100 Burjassot, Valencia, Spain
3. Departamento Química Orgánica, Universidad de Valencia, Dr. Moliner 50, E-46180 Burjassot, Valencia, Spain
Abstract
The reactivity of various b-aminoalcohols with diethyloxalate, in several reaction conditions, has been investigated. Lineal or cyclic derivatives were obtained depending on the nature of the solvent used and the starting material.
Keywords
tetrasubstituted oxalamide
morpholin-2,3-dione
theoretical calculations.
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