Acid promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base

التفاصيل البيبلوغرافية
العنوان: Acid promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base
المؤلفون: Paolo Righi, Emanuela Marotta, Francesco Tozzi, Claudio Paolucci, Goffredo Rosini, Francesca Boschi
المساهمون: G. Rosini, C. Paolucci, F. Boschi, E. Marotta, P. Righi, F. Tozzi
المصدر: Green Chemistry. 12:1747
بيانات النشر: Royal Society of Chemistry (RSC), 2010.
سنة النشر: 2010
مصطلحات موضوعية: chemistry.chemical_classification, Chiral auxiliary, INDUCED ASYMMETRIC TRANSFORMATION, CONVERGENT SYNTHESIS, Base (chemistry), Stereochemistry, TRANS-CHRYSANTHEMIC ACID, RING-CHAIN TAUTOMERISM, AROMATIC-ALDEHYDES, Convergent synthesis, Diastereomer, Oxazines, ENANTIOSELECTIVE ADDITION, Cleavage (embryo), Ring (chemistry), ARYL ALDEHYDES, Pollution, Aldehyde, OPTICAL RESOLUTION, chemistry.chemical_compound, chemistry, Environmental Chemistry, CHEMOENZYMATIC SYNTHESIS, RENIN INHIBITOR ALISKIREN
الوصف: Racemic alpha-epimerizable and unfunctionalized aldehydes have been converted into enantiomerically enriched mixtures through a sequence of (i) a conversion into the diastereoisomeric 3-substituted 1-phenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazines by reaction with the (R)- or (S)-1-(alpha-aminobenzyl)-2-naphthol (Betti's base), (ii) an acid promoted crystallization-induced diastereoisomer transformation (CIDT), and (iii) a clean cleavage of the dihydro-1,3-naphthoxazinic ring of the enriched diastereoisomer, easily collected by filtration, allowing the recovery of the enantiomerically enriched aldehydes and the chiral auxiliary.
وصف الملف: STAMPA
تدمد: 1463-9270
1463-9262
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3fdd0a0dad6ddb75d9f692def520fcfTest
https://doi.org/10.1039/c0gc00013bTest
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....e3fdd0a0dad6ddb75d9f692def520fcf
قاعدة البيانات: OpenAIRE