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    Öğe
    A Novel Methodology for the Asymmetric Synthesis of 2,3,5-Trisubstituted Piperazine Derivatives
    (Georg Thieme Verlag Kg, 2024) Beksultanova, Nurzhan; Ozdemir, Ozge; Cakir, Sidika Polat; Aygun, Muhittin; Dogan, Ozdemir
    Piperazines constitute an important structural feature of many pharmaceuticals. For the discovery of new drugs, the ability to modify the lead compound's structure is crucial. Herein, we provide an efficient method for the synthesis of chiral 2,3,5-trisubstituted piperazine structures. Our route enables the synthesis of several novel chiral aryl aziridinyl ketones that could be converted into aziridine-fused bicyclic imines. The reduction of these imines and the nucleophilic ring-opening reaction of the aziridine ring allowed us to synthesize highly functionalized piperazine derivatives.
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    Öğe
    Preparation and crystal structure of binuclear chloro{6-[[chloro(triphenylphosphine)platinum](mesitylimino)methyl]pyridin-2-yl}bis(triphenylphosphine)platinum(II)
    (Pergamon-Elsevier Science Ltd, 2008) Gunay, M. Emin; Dayan, Osman; Gokce, Aytac Gurhan; Aygun, Muhittin; Cetinkaya, Bekir; Buyukgungor, Orhan
    Treatment of N,N'-bis(mesityl)pyridine-2,6-carboxyimidoyldichloride, 1, in toluene solution with [Pt(PPh3)(4)] at 100 degrees C afforded a novel platinacyclic compound, 3, in 63% yield, instead of the expected compound 2. The molecular and crystal structures of the title compound, 3, have been determined by the single crystal X-ray diffraction technique. The coordination geometries around the Pt atoms are distorted square-planar. In the crystal structure, the molecules are linked by a pair of C-H center dot center dot center dot N hydrogen bonds into a centrosymmetric dinner with an R-2(2) (16) ring, centred at (1/2,1/2,1/2). (C) 2008 Elsevier Ltd. All rights reserved.