Stahl Lab
@Stahl_Lab
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Stahl Research Group in the Department of Chemistry at the University of Wisconsin-Madison
Madison, Wisconsin USA
Joined September 2020
Excited about our recent work! With @Stahl_Lab and a consortium of pharmaceutical companies, we built reactors to scale organic electrosynthesis. We found that mass transport and reaction mechanisms interact to define the reaction outcome! @ACSCentSci
pubs.acs.org
Organic electrosynthesis opens new avenues of reactivity and promises more sustainable practices in the preparation of fine chemicals and pharmaceuticals. The full value of this approach will be...
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Accessing monomers from lignin through carbon–carbon bond cleavage https://t.co/gl1Mm9rR5p A Review by Chad T. Palumbo, Erik T. Ouellette, Jie Zhu, Yuriy Román-Leshkov, Shannon S. Stahl & Gregg T. Beckham @NREL @MIT @MITChemE @UWMadison @yuriy_roman @Stahl_Lab
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.@UWMadison researchers – led by Shannon Stahl @Stahl_Lab and Thatcher Root – have developed a new process that could help make plant-based plastics and other alternatives to fossil fuels more economically viable. #WisconsinInnovates
energy.wisc.edu
The goal is to use lignin to produce valuable aromatic chemicals – hexagonal molecules such as benzene, toluene, and xylene – that are currently derived from petroleum as part of the refining...
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Excited to share this capstone of Eric Weeda’s thesis: aerobic oxidation method for lignin conversion to aromatics - continuous process readily generates aromatics on 100 g scale, with line-of-sight to more. @Joule_CP @UWEnergy @GLBioenergy @UWMadisonChem
https://t.co/6EkEzANLeg
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Zn and Mn are commonly used reductants in organic chemistry - but what are their redox potentials in organic solvent?!? Zhiming and Ruohan provide an answer and show why it matters in Ni XEC reactions. @UWMadisonChem @NatureChemistry (full access link) https://t.co/OQ3g77hvT7
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Asmaul and Tianxiao take us one step closer to eliminating peroxides and other undesirable oxidants in organic chemistry. Thanks to @DPSynthChemist @GSK for med chem contributions!
pubs.acs.org
Oxygen-atom transfer reactions are a prominent class of synthetic redox reactions that often use high-energy oxygen-atom donor reagents. Electrochemical methods can bypass these reagents by using...
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The Stahl Group is doing nickel chemistry?!? Just ask Zhiming, who just completed an entire PhD thesis on the topic. We're looking forward to your upcoming papers - congratulations, Zhiming!
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Couldn’t image a better mentor, committee member for many Stahl group students, and colleague. We’re still in a state of disbelief, but he’s going out at the top of his game!
Congratulations, Clark Landis, on your well-deserved retirement! Your dedication to advancing chemistry and everything you've given to this university will always be remembered. Thank you for everything! #Retirement #Congratulations #UWChem
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The Schreier Group is hiring a postdoc to work on exciting electrochemical scale-up and reactor design in collaboration with the pharmaceutical industry. We aim to fill the position by September 2024. Send your CV with publication list to schreierlab-openings@che.wisc.edu ⚡️🧪!
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We're celebrating Chair Clark Landis today! Professor Landis delivered his retirement seminar and we learned a lifetime of work cannot be summed up in just one hour. Congratulations on your retirement, Professor Landis!
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Finishing with flair, Melissa (Hopkins) Hall defended her thesis and leaves a legacy of exciting research. Congratulations, Melissa!! @UWMadisonChem
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@BagPhos had to start a new post here to avoid staring at that typo in the original TOC graphic :-(
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Excited to share Chris H's new Cu/nitroxyl oxidation method, converting cyclic 2° amines to lactams with direct access to metabolites and late-stage drug modification. Loved working with with #GSKChemistry team, @NikkiG_Conshy and @TessaColameta and Jen E. https://t.co/NCTvEC6Q9i
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Melissa and Maize (Davies group/Emory) show how an iron fuel cell electrocatalyst from @PajaritoPowder crushes the competition in this synthetic aerobic oxidation reaction - converting hydrazones to diazo compounds for C-H insertion and cyclopropanation
pubs.acs.org
Organic diazo compounds are versatile reagents in chemical synthesis and would benefit from improved synthetic accessibility, especially for larger scale applications. Here, we report a mild method...
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Congratulations to Professor Dan Suess, Professor Alison Wendlandt, and Professor Bin Zhang, who have all earned tenure effective July 1, 2024! https://t.co/JfIRPTgc92
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Online now: Neglected no longer: Selective C–H activation of the non-resonant C3 benzylic position of pyridine https://t.co/8RDUHas1ah
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Congratulations to two of our outstanding group members, Jesse Martinez and McKenna Goetz, for their @UWMadisonChem GSFLC Mentor Awards!! Thanks for all you do to support others! This recognition is so well deserved!
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Congratulations to our newest PhD, Eric Weeda, who gave an amazing talk on his thesis research on lignin deconstruction and valorization. @UWMadisonChem @GLBioenergy @UWEnergy
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