Tanja Kaehler - Catalysis

Author Information

Tanja Kaehler is affiliated with the Cardiff Catalysis Institute, School of Chemistry, Cardiff University, located in the Main Building, Park Place, Cardiff, CF10 3AT, Cymru/Wales, UK. Her research primarily focuses on the field of catalysis, with significant contributions to various sub-disciplines within this field.

Research Contributions

Tanja Kaehler has made significant contributions to the field of catalysis, as evidenced by her diverse range of research papers. Her work spans from comparative studies of chemical compounds, such as fluorinated triarylalanes and their borane counterparts, to the synthesis and functionalization of polycyclic aromatic hydrocarbons (PAHs). Notably, she has explored gold-catalyzed synthesis methods and selective vicinal diiodination processes. Additionally, Tanja has contributed to the development of new members in the azaborine family and innovative methods for synthesizing α-substituted sulfonamides via Brønsted acid-catalyzed C(sp3)-H bond functionalization of 2-alkylazaarenes.

Aliases

Tanja Kaehler is also known by the aliases "T. Kaehler" and "T Kaehler."

Publication and Citation Metrics

Metric	Value
Total Citations	43
h-index	3
Total Papers	8

Publications:

Comparative study of fluorinated triarylalanes and their borane counterparts

DOI: 10.1016/j.xcrp.2021.100595

Year: 2021

One tool to bring them all: Au-catalyzed synthesis of B,O- and B,N-doped PAHs from boronic and borinic acids†

DOI: 10.1039/d1sc00543j

Year: 2021

Selective Vicinal Diiodination of Polycyclic Aromatic Hydrocarbons

DOI: 10.1002/EJOC.202000954

Year: 2020

Introducing Perylene as a New Member to the Azaborine Family.

DOI: 10.1002/anie.201905823

Year: 2019

Introducing Perylene as a New Member to the Azaborine Family

DOI: 10.1002/ange.201905823

Year: 2019

3-Component synthesis of α-substituted sulfonamides via Brønsted acid-catalyzed C(sp(3))-H bond functionalization of 2-alkylazaarenes.

DOI: 10.1039/c6ob00108d

Year: 2016

3-Component Synthesis of α-Substituted Sulfonamides via Broensted Acid-Catalyzed C(sp3)-H Bond Functionalization of 2-Alkylazaarenes.

DOI: 10.1002/CHIN.201644058

Year: 2016

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