Enantioselective copper-catalyzed conjugate addition of diethylzinc to enones using new chiral P,N ligands composed of (S)-2-alkyl-2-aminoethylphosphines and α-substituted pyridines

التفاصيل البيبلوغرافية
العنوان: Enantioselective copper-catalyzed conjugate addition of diethylzinc to enones using new chiral P,N ligands composed of (S)-2-alkyl-2-aminoethylphosphines and α-substituted pyridines
المؤلفون: Toshiaki Morimoto, Masato Suzuki, Yoichi Yamaguchi, Akihito Saitoh
المصدر: Tetrahedron Letters. 41:10025-10029
بيانات النشر: Elsevier BV, 2000.
سنة النشر: 2000
مصطلحات موضوعية: chemistry.chemical_classification, Chalcone, Chemistry, Ligand, Organic Chemistry, Enantioselective synthesis, Diethylzinc, Biochemistry, Medicinal chemistry, chemistry.chemical_compound, Cyclohexenone, Drug Discovery, Copper catalyzed, Alkyl, Conjugate
الوصف: New P,N ligands prepared from (S)-2-alkyl-2-aminoethylphosphines and α-substituted pyridines are efficient chiral ligands for the copper-catalyzed conjugate addition of diethylzinc to 2-cyclohexen-1-one and chalcone. The best result (90–91% ee) for the cyclohexenone was obtained with Cu(OTf)2 (0.7–1 mol%) and a P,N ligand 4 derived from (S)-1-(diphenylphosphino)-3-methyl-2-butanamine and 6-methylpyridine-2-carboxaldehyde.
تدمد: 0040-4039
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a10eeabbf049b9eb5a86d10a791b18ec
https://doi.org/10.1016/s0040-4039(00)01789-5
حقوق: CLOSED
رقم الأكسشن: edsair.doi...........a10eeabbf049b9eb5a86d10a791b18ec
قاعدة البيانات: OpenAIRE