Yazarlar |
Şardan Melis
|
Serdar Sezer
|
Prof. Dr. Aslıhan GÜNEL
Ahi Evran Üniversitesi, Türkiye |
Mahinur Akkaya
Orta Doğu Teknik Üniversitesi, Türkiye |
Cihangir Tanyeli
Orta Doğu Teknik Üniversitesi, Türkiye |
Özet |
An efficient synthesis of racemic and both enantiomeric forms of heteroaryl substituted γ- and δ-lactone derivatives derived from allyl and homoallyl alcohol backbones has been accomplished via ring closing metathesis reaction. 2-Heteroaryl substituted allyl and homoallyl alcohols have been efficiently resolved through enzymatic method with high ee (97-99%) and known stereochemistry. Antimicrobial and antioxidant activities of target lactones were evaluated. © 2012 Published by Elsevier Ltd. |
Anahtar Kelimeler |
Asymmetric synthesis | Enzymatic resolution | Optically active lactones |
Makale Türü | Özgün Makale |
Makale Alt Türü | SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale |
Dergi Adı | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS |
Dergi ISSN | 0960-894X |
Dergi Tarandığı Indeksler | SSCI |
Makale Dili | İngilizce |
Basım Tarihi | 01-2011 |