Synthesis of C2-Symmetric Chiral Amino Alcohols: Their Usage as Organocatalysts for Enantioselective Opening of Epoxide Ring

Turgut, YilmazAral, TarikKarakaplan, MehmetDeniz, PinarHosgoren, Halil2024-04-242024-04-2420100039-79111532-2432https://doi.org/10.1080/00397910903419878https://hdl.handle.net/11468/16681A series of -amino alcohols derivatives were synthesized from (R)-2-amino-1-butanol and (S)-1,2-propanediol, and they have been used as organocatalaysts in the racemic ring opening of epoxide in good yields with high enantiomeric excess (up to 97%).eninfo:eu-repo/semantics/closedAccessAsymmetric Ring OpeningChiral Amino AlcoholEpoxideOrgano CatalysisSynthesis of C2-Symmetric Chiral Amino Alcohols: Their Usage as Organocatalysts for Enantioselective Opening of Epoxide RingSynthesis of C2-Symmetric Chiral Amino Alcohols: Their Usage as Organocatalysts for Enantioselective Opening of Epoxide RingArticle402233653377WOS:0002830701000102-s2.0-7795802952910.1080/00397910903419878Q2Q3