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Wengryniuk - Temple University Department of Chemistry

http://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.

Organic - Temple University Department of Chemistry

http://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.

Catalysis - Temple University Department of Chemistry

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 ...

Michael L. Klein wins prestigious John Scott Award

https://news.temple.edu/news/2021-12-14/michael-l-klein-wins-prestigious-john-scott-award

Michael L. Klein, dean of the College of Science and Technology (CST), has earned the prestigious John Scott Award for developing algorithms for the computational simulation of biological systems and the development of antimicrobial peptides.

CONTENTdm - digital.library.temple.edu

https://digital.library.temple.edu/digital/collection/p245801coll10/id/577805/

Approximately two-thirds of all antibiotics are derived from natural products, so the structural modification of natural products-derived antibiotics by either semi- or total synthesis is a highly successful strategy for discovering novel drugs to address bacterial resistance. My Ph.D. research project comprises of analog development for three ...

Semi-Synthesis of Melodinine, Taberyunine, and Melosuavine Bis-Indole ...

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.