Bianka Kótai

Eötvös Loránd University — Hungary

Chemistry · Physical Sciences

12h-index907citations42works1.72yr avg
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Research Topics

Organoboron and organosilicon chemistry(21), Crystallization and Solubility Studies(14), X-ray Diffraction in Crystallography(14), Asymmetric Synthesis and Catalysis(8), Crystallography and molecular interactions(8)

Publications42 total

Convenient Partial Reduction of CO<sub>2</sub> to a Useful C<sub>1</sub> Building Block: Efficient Access to <sup>13</sup>C‐Labelled N‐Heterocyclic Carbenes
ChemCatChem·2024Open Access
Author response for "Illuminating the Multiple Lewis Acidity of Triaryl-Boranes via Atropisomeric Dative Adducts"
2024
Author response for "Illuminating the Multiple Lewis Acidity of Triaryl-Boranes via Atropisomeric Dative Adducts"
2024
Author response for "Synergetic effects on the capture and release of CO2 using guanidine and amidine superbases"
2024
Stereocontrol via Propeller Chirality in FLP‐Catalyzed Asymmetric Hydrogenation
Chemistry - A European Journal·2024· 2 citedOpen Access
Single-Center, but Multipotent Lewis acids: Illuminating the Multiple Lewis Acidity of Triaryl-Boranes via Atropisomeric Dative Adducts
2024· 1 citedOpen Access
Stereocontrol via Propeller Chirality in FLP-Catalyzed Asymmetric Hydrogenation
2024· 1 citedOpen Access
Single-Center, but Multipotent Lewis acids: Illuminating the Multiple Lewis Acidity of Triaryl-Boranes via Atropisomeric Dative Adducts
2024· 2 citedOpen Access
Stereocontrol via Propeller Chirality in FLP-Catalyzed Asymmetric Hydrogenation
2024· 1 citedOpen Access
Synergetic effects on the capture and release of CO <sub>2</sub> using guanidine and amidine superbases
RSC Sustainability·2024· 8 citedOpen Access
Illuminating the multiple Lewis acidity of triaryl-boranes <i>via</i> atropisomeric dative adducts
Chemical Science·2024· 4 citedOpen Access
CCDC 2007899: Experimental Crystal Structure Determination
The Cambridge Structural Database·2021Open Access
CCDC 2007900: Experimental Crystal Structure Determination
The Cambridge Structural Database·2021Open Access
Origin of Stereoselectivity in FLP-Catalyzed Asymmetric Hydrogenation of Imines
ACS Catalysis·2020· 35 citedOpen Access
Expanding the Boundaries of Water‐Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls
Angewandte Chemie·2017· 21 cited
Expanding the Boundaries of Water‐Tolerant Frustrated Lewis Pair Hydrogenation: Enhanced Back Strain in the Lewis Acid Enables the Reductive Amination of Carbonyls
Angewandte Chemie International Edition·2017· 100 cited
Correlating electronic and catalytic properties of frustrated Lewis pairs for imine hydrogenation
Journal of Organometallic Chemistry·2017· 25 cited
CCDC 912583: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
CCDC 912585: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
CCDC 912584: Experimental Crystal Structure Determination
The Cambridge Structural Database·2017Open Access
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Frequent Co-authors

Imre Pápai(41), Timo Repo(26), Martin Nieger(23), Konstantin Chernichenko(19), Tibor Soós(10), Markus Lindqvist(9), Markku Leskelä(9), Andrea Hamza(9), Éva Dorkó(9), Kristina Sorochkina(8), Attila Domján(8), Gergely Laczkó(8), Márk Szabó(7), Tamás Földes(7), Владимир В. Живонитко(6), Sami Heikkinen(6), Katja Borre(5), Kirill Axenov(5), Benjamin Kovács(5), Tamás Holczbauer(5)