Synthesis of C2-Symmetric Chiral Amino Alcohols: Their Usage as Organocatalysts for Enantioselective Opening of Epoxide Ring
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Tarih
2010
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Taylor & Francis Inc
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
A 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%).
Açıklama
Anahtar Kelimeler
Asymmetric Ring Opening, Chiral Amino Alcohol, Epoxide, Organo Catalysis
Kaynak
Synthetic Communications
WoS Q Değeri
Q3
Scopus Q Değeri
Q2
Cilt
40
Sayı
22
