https://chem.cst.temple.edu/wengryniuk.html
Representative research areas include C–H activation, asymmetric C–C bond formation, novel methods to access carbon, oxygen, and nitrogen containing ring systems, and the synthesis of natural products targeting cancer metastasis.
https://chem.cst.temple.edu/organic.html
Organic chemistry. Inorganic, Organic. Hypervalent iodine chemistry, approaches to medium-sized ring systems, C-H activation, synthesis of bioactive natural products.
http://chem.cst.temple.edu/catalysis.html
Catalysis. Inorganic, Organic. Hypervalent iodine chemistry, approaches to medium-sized ring systems, C-H activation, synthesis of bioactive natural products. Synthetic and mechanistic inorganic and bioinorganic chemistry and crystallography: multi-metal molecular clusters and solid-state systems of fundamental chemical and biological interest ...
https://scholarshare.temple.edu/handle/20.500.12613/7731
Abstract The first semi-synthesis of (-)-melodinine K was completed from the monoterpene indole alkaloid (-)-tabersonine through regioselective enzymatic hydroxylation and Polonovski-Potier coupling.
http://chem.cst.temple.edu/synthesis.html
Synthesis. Inorganic, Organic. Hypervalent iodine chemistry, approaches to medium-sized ring systems, C-H activation, synthesis of bioactive natural products. Synthetic and mechanistic inorganic and bioinorganic chemistry and crystallography: multi-metal molecular clusters and solid-state systems of fundamental chemical and biological interest ...
https://cst.temple.edu/news/2021/07/memoriam-dr-rodrigo-andrade
The central theme of Rod's research at Temple University was the asymmetric synthesis of architecturally complex natural products, focusing on the total synthesis of two families of complex and biologically active natural products, macrolide antibiotics and indole alkaloids.