Browsing by Author "Yenidede, Duygu"

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Chemoenzymatic Synthesis of Novel 1,4-Disubstituted 1,2,3-Triazole Derivatives From 2-Heteroaryl Substituted Homopropargyl Alcohols
(Pergamon-elsevier Science Ltd, 2015) Buyukadali, Nalan Nuriye; Seven, Semih; Aslan, Nezir; Yenidede, Duygu; Gumus, Aysegal
The one-pot synthesis of novel 1,4-disubstituted 1,2,3-triazoles from homopropargyl alcohol backbones is described. The key intermediates 2-benzothiophenyl la and 2-benzofuranyl lb substituted homopropargyl alcohols were synthesized starting from their corresponding carboxyaldehyde derivatives. The racemic heteroaryl-substituted homopropargyl alcohol derivatives are successfully resolved to give the corresponding enantiopure acetates and the alcohols with 84-99% ee by applying chemoenzymatic methods using various lipases. Enantiomerically enriched homopropargyl alcohol derivatives were reacted with various aromatic and aliphatic halides and sodium azide via a one-pot synthesis method and novel chiral benzothiophenyltriazoles 3a-9a and benzofuranyltriazoles 3b-9b were constructed without the isolation of potentially unstable organic azide intermediates. (C) 2015 Elsevier Ltd. All rights reserved.
Isoquinoline-Substituted Hybrid Compounds: Synthesis and Computational Studies
(Mdpi, 2016) Gumus, Aysegul; Gumus, Selcuk; Yenidede, Duygu
The one-pot synthesis of novel 1,4-disubstituted 1,2,3-triazoles from isoquinoline-substituted homopropargyl alcohol backbone is described (42-88% yields). A ring closing metathesis (RCM) reaction and an intramolecular Pauson-Khand reaction (PKR) of enyne system derived from a homopropargyl alcohol backbone to afford the corresponding isoquinoline-substituted dihydropyran and cyclopentenone-pyran, respectively, are also described (54% and 78% yields). Information about the structural, electronic and physico-chemical properties of the novel compounds, obtained by density functional theory application, is also reported.
Isoquinoline-Substituted Triazole and Pyran Derivatives: Synthesis and Computational Studies
(Tubitak Scientific & Technological Research Council Turkey, 2016) Yenidede, Duygu; Gumus, Selcuk; Gumus, Aysegul
The one-pot synthesis of novel 1,4-disubstituted 1,2,3-triazoles from isoquinoline-substituted homopropargyl alcohol backbone is described (42%-88% yields). A ring closing metathesis reaction and an intramolecular Pauson-Khand reaction of enyne system derived from a homopropargyl alcohol backbone to afford the corresponding isoquinoline-substituted dihydropyran and cyclopentenone-pyran, respectively, are also described (54% and 78% yields). Information about the structural, electronic, and physico-chemical properties of the novel compounds, obtained by density functional theory application, is also reported.
Kiral 1,4-disübstitüe 1,2,3-triazollerin Kemoenzimatik One- Pot Sentezi ve Tepkime Mekanizmasının Teorik Olarak İncelenmesi
(2016) Gümüş, Selçuk; Gümüş, Ayşegül; Yenidede, Duygu