ChemInform Abstract: First Asymmetric Synthesis of a 6-Alkoxy-5,6-dihydro-1,3-oxazine: A Promising Enantioselective Route to β-Amido Aldehydes

التفاصيل البيبلوغرافية
العنوان: ChemInform Abstract: First Asymmetric Synthesis of a 6-Alkoxy-5,6-dihydro-1,3-oxazine: A Promising Enantioselective Route to β-Amido Aldehydes
المؤلفون: Loic Toupet, Patricia Gizecki, Gilles Dujardin, Robert Dhal
المصدر: ChemInform. 31
بيانات النشر: Wiley, 2010.
سنة النشر: 2010
مصطلحات موضوعية: chemistry.chemical_compound, Hydrolysis, Enantiopure drug, chemistry, Imine, Alkoxy group, Enantioselective synthesis, Organic chemistry, General Medicine
الوصف: The 1,3-oxazine route to enantiopure β-amido aldehydes was investigated. Heterocycloaddition of the N-acyl imine 1 with (R)-O-vinylpantolactone provided the stable dihydroxazine 4c. High diastereocontrols were observed when using Yb(fod)3-catalyzed or SnCl4-mediated conditions, thus leading after quantitative hydrolysis to (R)-N-benzoyl-3-phenylpropanal with >98% ee.
تدمد: 1522-2667
0931-7597
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9afef4b202d0c98baa6a81d22d934d62
https://doi.org/10.1002/chin.200025163
حقوق: CLOSED
رقم الأكسشن: edsair.doi...........9afef4b202d0c98baa6a81d22d934d62
قاعدة البيانات: OpenAIRE