Eric Welin Email and Phone Number
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I was born in central Ohio and attended the Ohio State University, where I graduated with a B.S. in Chemistry in 2010. I moved east to pursue my graduate studies working with Prof. David MacMillan at Princeton University pursuing new conceptual developments in the field of Photoredox Catalysis. After defending my thesis in October of 2015, I moved to the west coast to work as a Postdoctoral Researcher with Prof. Brian Stoltz at Caltech pursuing the total synthesis of the anticancer alkaloids Jorunnamycin A and Jorumycin. After starting an academic career at UT Dallas, I ultimately chose to realign my life and joined BMS in San Diego as a Scientist in Small Molecule Drug Discovery.
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Senior ScientistBristol Myers Squibb Mar 2021 - PresentSan Diego, California, United StatesI have worked to develop novel orally bioavailable CELMoD protein degraders and antibody-drug conjugates. I have experience using AI/ML models to optimize drug candidates to improve ADME/PK properties to maximize therapeutic windows to benefit patients. -
Assistant ProfessorThe University Of Texas At Dallas Sep 2019 - Mar 2021Richardson, TxI have established an organic chemistry laboratory at UT Dallas to pursue the total synthesis of natural products, with a focus on biologically active molecules. We have received funding from the Cancer Prevention & Research Institute of Texas (CPRIT) to pursue the total synthesis of a family of natural products and subsequently perform a series of hypothesis-driven medicinal chemistry studies. -
Postdoctoral FellowCaltech Nov 2015 - Aug 2019Pasadena, CaI led a team of synthetic chemists that completed the enantioselective total syntheses of jorunnamycin A and jorumycin, two anti-cancer alkaloid natural products. This highly collaborative effort also involved collaboration with medicinal chemists and cancer biologists at the University of California, Los Angeles for the design and testing of non-natural analogs of the natural products. We performed basic SAR studies and discovered that selective deletion of one hydroxyl group produces more broad cytotoxic effects than the fully decorated motifs. -
Graduate StudentPrinceton University Jul 2010 - Oct 2015I graduated from the lab of David MacMillan working in the field of catalysis and organic methods development. I worked as a team to develop an enantioselective cyanoalkylation reaction, and later I led a team that discovered a novel C–O coupling reaction between aryl bromides and carboxylate nucleophiles mediated by nickel and iridium catalysts. Through collaborative studies with chemists at Michigan State University, we showed that the reaction most likely operated via energy transfer-induced C–O reductive elimination from photoexcited nickel(II).
Eric Welin Skills
Eric Welin Education Details
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Princeton UniversityOrganic Chemistry -
The Ohio State UniversityChemistry
Frequently Asked Questions about Eric Welin
What company does Eric Welin work for?
Eric Welin works for Bristol Myers Squibb
What is Eric Welin's role at the current company?
Eric Welin's current role is Former prof turned medicinal chemist in San Diego.
What is Eric Welin's email address?
Eric Welin's email address is ew****@****ech.edu
What schools did Eric Welin attend?
Eric Welin attended Princeton University, The Ohio State University.
What skills is Eric Welin known for?
Eric Welin has skills like Organic Synthesis, Mass Spectrometry, Nmr Spectroscopy, Asymmetric Catalysis, Organic Chemistry, Hplc, Chemistry, Catalysis, Nmr, Spectroscopy, Nuclear Magnetic Resonance.
Who are Eric Welin's colleagues?
Eric Welin's colleagues are Chiyoko Kanzaki, Luis Castro, Jesus Landron, Daniel Mercado Salerno, Sean Vaughn, Fran Morrison, Carlos Johnson, M.ed..
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