Synthesis Of Bicyclo 2 2 2 OCTANE 2 3 5 6 7 8 Hexols Bishomoinositols New Glycosidase Inhibitors
 
Yazarlar (3)
Arif Baran Middle East Technical University (Metu), Türkiye
Prof. Dr. Aslıhan GÜNEL Sinop Üniversitesi, Türkiye
Metin Balcı Middle East Technical University (Metu), Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Journal of Organic Chemistry
Dergi ISSN 0022-3263 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SSCI
Makale Dili İngilizce Basım Tarihi 02-2008
Kabul Tarihi 12-04-2026 Yayınlanma Tarihi
Cilt / Sayı / Sayfa 73 / 12 / 4370–4375 DOI 10.1021/jo800553u
Makale Linki https://hdl.handle.net/11511/57615
Özet
For the construction of the bicyclo[2.2.2]octane skeleton, 2,2-dimethyl-3a,7a-dihydro-1,3-benzodioxole was reacted with vinylene carbonate to give two isomeric cycloadditon products having the bicyclo[2.2.2]octane skeleton. Hydrolysis of the ketal ring and the opening of the carbonate functionality, followed by hydroxylation of the remaining double bond resulted in the formation of a symmetrical hexol. Epoxidation of the double bond in the cycloaddition products and the subsequent ring-opening reactions produce two additional hexol derivatives. One of the synthesized molecules exhibited enzyme-specific inhibition against α-glycosidase.
Anahtar Kelimeler
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Google Scholar 32
Scopus 1
Synthesis Of Bicyclo 2 2 2 OCTANE 2 3 5 6 7 8 Hexols Bishomoinositols New Glycosidase Inhibitors

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