https://cst.temple.edu/about/faculty-staff/sarah-wengryniuk
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://pharmacy.temple.edu/magidabougharbia
The group’s research further focuses on: (a) the use of receptor homology, bioisosteric replacement strategies, rational and structure-based drug design approaches; (b) utilizing natural products as a unique resource for discovering innovative therapeutics; (c) applying enabling technology platforms and in vitro ADME to evaluate drug-like ...
https://sites.temple.edu/beaudry/publications-2/
21. “The Nature of Persistent Conformational Chirality, Racemization Mechanisms, and Predictions in Diarylether Heptanoid Cyclophane Natural Products” Ommidala Pattawong, M. Quamar Salih, Nicholas T. Rosson, Chris Beaudry and Paul Cheong Org. Biomol. Chem.,2014, 12, 3303-3309.
https://liberalarts.temple.edu/research/labs-centers-and-institutes/center-sustainable-communities
Our new PSM and Graduate Certificate offerings train professionals in sustainability science so they can address challenges including unequal impacts of climate change, biodiversity loss, clean energy transitions and resilient cities.
https://engineering.temple.edu/research/labs-centers/civil-environmental-engineering-labs
Dedicated to the investigation of physicochemical processes, environmental chemistry, remediation, and fate & transport, our lab performs experimental research on societally and environmentally relevant issues, and our research addresses both natural and engineered treatment systems.
https://scholarshare.temple.edu/bitstream/handle/20.500.12613/6308/Dalton-JournalArticle-2006.pdf?sequence=1
Abstract: Morphine (1) and its O-methylated analogue codeine (2), analgesic alkaloids of the opium poppy (Papaver Somniferium), have been targets of organic chemists engaged in synthetic activities for at least half a century.
https://events.temple.edu/mingji-dai-chemistry-innovation-and-biological-discovery-through-natural-product-total-synthesis
This talk will focus on our recent efforts in function and efficiency-driven total synthesis of medicinally important natural products. The target molecules include macrolides, alkaloids, and polycyclic diterpenoids.
https://tyler.temple.edu/faculty/sasha-eisenman-phd
Sasha Eisenman is a botanist and horticulturist with a diverse portfolio of research projects. Currently, his primary area of research is on the survival, health and ecophysiological responses of plants in green infrastructure systems (tree trenches, bioswales and rain gardens).
https://cst.temple.edu/about/faculty-staff/christopher-beaudry
The Beaudry group is broadly interested in natural products and creating methods for their synthesis. The natural products we target are from every major natural product class. Moreover, the reactions we develop are diverse in terms of mechanism; we have created new pericyclic, ionic, and radical reactions.
https://sites.temple.edu/beaudry/dr-beaudry/
His graduate work was centered around the biomimetic total synthesis of the polyketide natural products SNF4435C and SNF4435D. Chris conducted postdoctoral research in the group of Larry Overman at the University of California, Irvine. In Irvine he worked the synthesis of aplyviolene and macfarlandin E, two rearranged spongian diterpenes.