Highly diastereoselective access to polyfunctionalized 1,3- oxazines promoted by Brønsted/Lewis acids
| Autor: | Philippe Geoffroy, Michel Miesch, Clovis Peter |
|---|---|
| Přispěvatelé: | univOAK, Archive ouverte, Institut de Chimie de Strasbourg, Centre National de la Recherche Scientifique (CNRS)-Université Louis Pasteur - Strasbourg I-Institut de Chimie du CNRS (INC), Laboratoire de Chimie Quantique, Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC) |
| Jazyk: | angličtina |
| Rok vydání: | 2018 |
| Předmět: |
chemistry.chemical_classification
[CHIM.ORGA]Chemical Sciences/Organic chemistry 010405 organic chemistry Organic Chemistry Oxazines 010402 general chemistry [CHIM.ORGA] Chemical Sciences/Organic chemistry 01 natural sciences 0104 chemical sciences 3. Good health Catalysis chemistry Organic chemistry Lewis acids and bases |
| Zdroj: | Organic Chemistry Frontiers Organic Chemistry Frontiers, Royal Society of Chemistry, 2018, 5, pp.566-570 |
| ISSN: | 2052-4129 |
| Popis: | The Bronsted/Lewis acid catalyzed reaction of pyrrolidone, piperidone and isoindolinone derivatives tethered to α,β-unsaturated ketones or aldehydes afforded exclusively polyfunctionalized 1,3-oxazines with high diastereoselectivities and in high yields. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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