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Wengryniuk - Temple University Department of Chemistry

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.

Organic - Temple University Department of Chemistry

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. TEMPLE UNIVERSITY.

Medicinal - Temple University Department of Chemistry

https://chem.cst.temple.edu/medicinal.html

Metal uptake and transport, potential therapeutic applications, and biomineralization. Hypervalent iodine chemistry, approaches to medium-sized ring systems, C-H activation, synthesis of bioactive natural products. TEMPLE UNIVERSITY.

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.

The A-Team | The Andrade Lab - Sites

https://sites.temple.edu/andradelab/the-a-team/

Po-Cheng joined the Andrade Lab in 2016 and currently works on novel N-sulfinyl imine and N-sulfinylmetallodienamine methodology including the Domino Michael/Mannich reaction, Diels-Alder reaction, and Vinylogous Aldol reaction, which are utilized toward the synthesis of complex natural products such as (+)-ibogamine.

Photocycloaddition of Conjugated Enynes and its Application in Natural ...

https://digital.library.temple.edu/digital/collection/p245801coll10/id/374437/

The synthetic utility of enyne photocycloaddition was applied in the synthesis of the cyclooctanoid containing natural product, (+)-dactylol. The intramolecular enyne – 2-pyrone [4+4] photocycloaddition-isomerization gave a lactone bridged-cyclooctanoid product which serves as an advanced intermediate for sesquiterpene synthesis.