Synthesis and biological evaluation of optically active conjugated and lactone derivatives
     
Yazarlar (5)
Melis Ardan
Middle East Technical University (Metu), Türkiye
Serdar Sezer
Middle East Technical University (Metu), Türkiye
Prof. Dr. Aslıhan GÜNEL Kırşehir Ahi Evran Üniversitesi, Türkiye
Mahinur Akkaya
Middle East Technical University (Metu), Türkiye
Cihangir Tanyeli
Middle East Technical University (Metu), Türkiye
Makale Türü Açık Erişim Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Bioorganic and Medicinal Chemistry Letters
Dergi ISSN 0960-894X Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SSCI
Makale Dili İngilizce Basım Tarihi 01-2011
Cilt / Sayı / Sayfa 22 / 18 / 5814–5818 DOI 10.1016/j.bmcl.2012.07.090
Makale Linki https://hdl.handle.net/11511/41482
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