1,2,3,5- tetrasubstitue pirol türevlerinin 5-exo-dig tipi halkalaşma tepkimesi ile sentezi ve ferrosen türevlerinin stereoseçici olarak fonksiyonlandırılması


Tezin Türü: Yüksek Lisans

Tezin Yürütüldüğü Kurum: Orta Doğu Teknik Üniversitesi, Fen Edebiyat Fakültesi, Kimya Bölümü, Türkiye

Tezin Onay Tarihi: 2005

Tezin Dili: İngilizce

Öğrenci: Metin Kayalar

Danışman: AYHAN SITKI DEMİR

Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu

Özet:

A convenient and new method for the synthesis of 1,2,3,5-tetrasubstituted pyrrole derivatives starting from 1,3,-dicarbonyl compounds through acid catalyzed cyclization reaction is described. Alkylation of 1,3-dicarbonyl compound with propargyl bromide followed by one step cyclization with the introduction of primary amines in the presence of catalytic amount of triflouroacetic acid (TFA) affords the corresponding pyrrole derivatives in high yields. The investigations on the studies of developing a new method for catalytic and stereoselective functionalisation of ferrocene derivatives were summarized. Functionalisation studies were carried out in three main strategy the first one of which is carboxylation, second one is arylation and the last one is oxidative cross-coupling with a, β-unsaturated carbonyl compounds.