https://hdl.handle.net/20.500.12619/1009 2026-04-13T17:51:36Z https://hdl.handle.net/20.500.12619/3918 Bibliometric Analysis of Maliye Dergisi (Journal of Finance): The Period of 2007-2016 Beşel, Furkan; Yardımcıoğlu, Fatih The present study aims to determine the transformation of public finance by analyzing 330 articles which were published in Maliye Dergisi between the years 2007-2016 through bibliometric analysis. Furthermore, the studies which were published in Maliye Dergisi which has an important place in the Turkish public finance will be evaluated in terms of different variables as a result of the analysis. The most interesting result of the study is the increase of empirical studies in the field of public finance in the recent years. 2017-01-01T00:00:00Z https://hdl.handle.net/20.500.12619/3913 A new and efficient synthesis of indenone Zengin, Mustafa; Balci, Mustafa Reaction of dichloroketone 2 with NEt3 gave indenone (4) in high yield. Catodic reaction of 2 in the presence of C/Pt electrodes afforded the rearranged product 3 in high yield besides a small amount of chlorohydroxyketone 5. Reaction of rearranged dichloroketone 3 with NEt3 provided indenone (4) as the sole product. The mechanism of these reaction was discussed. 2001-01-01T00:00:00Z https://hdl.handle.net/20.500.12619/3914 Functionalisation of indene Tutar, Ahmet; Çakmak, Ömer; Balci, Mustafa Dibromo- and tribromoindane were synthesised by bromination of indene. Treatment of dibromo- and tribromoindane with various silver salts (silver acetate, perchlorate, sulfate and nitrate) in different solvents opened up an entry to the synthesis of various di- and tri-substituted indane derivatives. 2006-01-01T00:00:00Z https://hdl.handle.net/20.500.12619/3916 Stereospecific synthesis of a DL-gala-aminoquercitol derivative Kurbanoğlu, Namudar İzzet; Kılıç, Harun; Balci, Mustafa A new aminoquercitol derivative was synthesized starting from 1,4-cyclohexadiene. Photooxygenation of cyclohexa-1,4-diene afforded anti-2,3-dioxabicyclo[2.2.2]oct-7-en-5-yl hydroperoxicle as the main product. The formed hydroperoxy endoperoxide was reduced with LiAlH(4) to produce anti-2,3-dioxabicyclo[2.2.2]oct-7-en-5-ol. Protection of alcohol with acetyl chloride followed by reduction of the endoperoxide with thiourea, and then palladium-catalyzed ionization/cyclization reaction gave an oxazolidinone derivative. Hydrolysis of the oxazolidinone ring and acetylation gave an amino compound. Oxidation of the double bond in the amino compound with OsO(4) followed by acetylation gave the amino tetraacetate and removal of the acetate groups furnished the desired aminoquercitol whose exact configuration was determined by X-ray diffraction analysis. (C) 2010 Elsevier Ltd. All rights reserved. 2010-01-01T00:00:00Z