Publications

2021

Aldol Reactions of Conformationally Stable Axially Chiral Thiohydantoin Derivatives

Ozbek Sari, S., Erdik Bacak, M., Dogan, I.
ACS Omega , 6 , 27823-27832 , 2021 , Impact Factor: 3.512 , Q1

Using Atomic Charges to Describe the pKa of Carboxylic Acids

Haslak, Z.P., Zareb, S., Dogan, I., Aviyente, V., Monard, G.
Journal of Chemical Information and Modeling , 61 (6) , 2733-2743 , 2021 , Impact Factor: 4.549 , Q1

An Acyclic Diaminocarbene Complex of Platinum Formedby Desulfurization of 1,3-Bis(3-methylpyridin-2-yl)thiourea

Bulak, E., Dogan, I., Varnali, T., Schwederski, B., Gunal Erol, S., Lonnecke, P., Bubrin, M., Kaim, W.
European Journal of Inorganic Chemistry , 2425-2432 , 2021 , Impact Factor: 2.524 , Q2

2020

Synthesis of thiazol‐2‐imines from the reduction of single enantiomer 2‐imino‐thiazolidin‐4‐ones followed by a spontaneous water elimination

Teke Tuncel, S., Dogan, I.
Chirality , 32 , 866-875 , 2020 , Impact Factor: 1.910 , Q2

Elucidation of the Atroposelectivity in the Synthesis of Axially Chiral Thiohydantoin Derivatives

Haslak, Z. P., Cinar Agopcan, S., Ozbek Sarigul, Monard, G., Dogan, I., Aviyente, V.
Organic & Biomolecular Chemistry , 18 , 2233-2241 , 2020 , Impact Factor: 3.274 , Q1

Axially Chiral Hemiaminals From Nonracemic α‐amino Acid Derivatives (Thiohydantoins): Synthesis And Isomer Identification

Sarigul Ozbek, S., Dogan, I.
Chirality , 32 , 1299-1310 , 2020 , Impact Factor: 1.910 , Q2

Enantiodiscrimination of carboxylic acids using single enantiomer thioureas as chiral solvating agents

Gunal Erol, S., Tuncel Teke, Dogan, I.
Tetrahedron , 76 , 131141 , 2020 , Impact Factor: 2.457 , Q2

2019

Thioureas and their cyclized derivatives: Synthesis, conformational analysis and antimicrobial evaluation

Tuncel Teke, S., Gunal Erol, Ekizoglu, M., Kelekci Gokhan, N., Erdem, Bulak, E., Frey, W., Dogan, I.
Journal of Molecular Structure , 1179 , 40-56 , 2019 , Impact Factor: 3.196 , Q3

2018

Asymmetric Synthesis, Molecular Modeling and Biological Evaluation of 5-methyl-3-aryloxazolidine-2,4-dione Enantiomers as Monoamine Oxidase (MAO) Inhibitors

Erol Gunal, S., Tuncel, S., Kelekci, N., Ucar, G., Dursun, B., Erdem, Dogan, I.
Bioorganic Chemistry , 77 , 608-618 , 2018 , Impact Factor: 3.231 , Q2

2016

Atroposelective Synthesis of Axially Chiral Thiohydantoin Derivatives

Sarigul, S., Dogan, I.
Journal of Organic Chemistry , 81 (14) , 5895-5902 , 2016 , Impact Factor: 4.785 , Q1

Synthesis of Stable Tetrahedral Intermediates (Hemiaminals) and Kinetics of their Conversion to Thiazol-2-imines

Erol Gunal, S., Sabuncu Gurses, G., Sag Erdem, Dogan, I.
Tetrahedron , 72 (17) , 2122-2131 , 2016 , Impact Factor: 2.641 , Q2

2015

Elucidating the Structural Isomerism of Fluorescent Strigolactone Analogue CISA-1

Goossens, H., Heugebaert, T.S.A., Dereli, B., Van Overtveldt, M., Karahan, O., Dogan, I., Waroquier, M., Van Speybroeck, V., Aviyente, V., Catak, S., Stevens, C.V.
European Journal of Organic Chemistry , 2016 (6) , 1211-1217 , 2015 , Impact Factor: 3.065 , Q1

2014

The origin of exo-stereoselectivity of norbornene in hetero Diels-Alder reactions

Agopcan Cinar, S., Ercan, Erol Gunal, Dogan, I., Aviyente, V.
12 (40) , 8079-8086 , 2014 , Impact Factor: 3.487 , Q1

Axially chiral pyridine compounds: synthesis, chiral separations and determination of protonation dependent barriers to hindered rotation

Isikgor, F.H., Erol, S., Dogan, I.
Tetrahedron: Asymmetry , 25 (5) , 449–456 , 2014 , Impact Factor: 2.143 , Q2

2013

exo-Selective inverse-electron-demand hetero Diels–Alder reactions of norbornene with 5-benzylidine-2-arylimino-3-aryl-thiazolidine-4-thiones at room temperature

Erol, S., Dogan, I.
Tetrahedron , 69 (4) , 1337–1344 , 2013 , Impact Factor: 2.803 , Q2

2012

Solvent-Catalyzed Ring–Chain–Ring Tautomerization in Axially Chiral Compounds

Yildirim, A., Konuklar, F. A. S., Catak, S., Speybroeck, V. V., Waroquier, M., Dogan, I., Aviyente, V.
Chemistry - A European Journal , 18 (40) , 12725-12732 , 2012 , Impact Factor: 5.831 , Q1

Determination of barriers to rotation of axially chiral 5-methyl-2-(o-aryl)imino-3-(o-aryl)thiazolidine-4-ones

Erol, S., Dogan, I.
Chirality , 24 (6) , 493-498 , 2012 , Impact Factor: 1.72 , Q2

Stereochemical assignments of aldol products of 2-arylimino-3-aryl-thiazolidine-4-ones by 1H NMR

Erol, S., Dogan, I.
Magnetic Resonance in Chemistry , 50 (5) , 402-405 , 2012 , Impact Factor: 1.53 , Q2

2010

Stereoselective lithiation and alkylation and aldol reactions of chiral 5-methyl-3-(o-aryl)-oxazolidinones

Demir, O. O., Dogan, I.
Tetrahedron: Asymmetry , 21 (20) , 2455-2464 , 2010 , Impact Factor: 2.115 , Q2

Axially chiral N-(o-aryl)-4-hydroxy-2-oxazolidinone derivatives from diastereoselective reduction of N-(o-aryl)-2,4-oxazolidinediones: thermally interconvertible atropisomers via ring-chain-ring tautomerization

Demir, O. O., Dogan, I.
Chirality , 22 (7) , 641-654 , 2010 , Impact Factor: 1.720 , Q2