Weix Group
@weixgroup
Weix Group at UW-Madison. Primarily student run, with the occasional DJW tweet. Mostly group news. @weixgroup.bsky.social
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Perhaps belatedly, we are shutting down on twitter - thank you to all the chemists out there who participated. It was pretty awesome while it lasted! Times change and so must we. Check out our website for the latest news as we change up how we share things. -DJW
Congratulations Dr. Lauren Ehehalt on a fantastic thesis defense! We're so excited to see all your future work at @EastmanChemCo 🥳🎉🎓
Our work on the translation of Nickel-Catalyzed C(sp2)–C(sp3) Cross-Electrophile Coupling to Non-Amide Solvents is now online in @JOC_OL! Congrats to Brett, Julianna, Michelle, and wonderful collaborators at @NovartisScience. Check it out! doi.org/10.1021/acs.or…
Honoring Excellence in Chemistry Teaching! Congratulations to our 2025 Chemistry Teaching Award winners! Thank you for all of your hard work! Learn more here loom.ly/J00JlKM
Congrats to Julianna for receiving an Outstanding Chemistry Teaching Assistant Award for your work with Chem 636 and the NMR facilities! Well deserved! 🎉
Cross-Electrophile Coupling to Form Sterically Hindered C(sp2)–C(sp3) Bonds: Ni and Co Afford Complementary Reactivity | Journal of the American Chemical Society @UWMadison @UWMadisonChem @weixgroup @TotalSyntheses pubs.acs.org/doi/10.1021/ja…
Our work on Ni- and Co-catalyzed Cross-Electrophile Coupling to Form Sterically Hindered C(sp2)–C(sp3) Bonds is now online at @J_A_C_S! Congrats to Tianrui, Anthony, Kasturi, and our collaborators Madeline (@KozlowskiMarisa) and @NovartisScience doi.org/10.1021/jacs.4…
Our work on in-situ generation of alkyl chlorides using Ghosez’s reagent and coupling with aryl chlorides is now online at @JOC_OL Congrats Ben! Check it out! doi.org/10.1021/acs.or…
Ni-Cat Cross-Electrophile Coupling of ArOTf/AlkHal: Mechanism-Informed Design of General Conditions | Journal of the American Chemical Society @UWMadisonChem @UWMadison @TotalSyntheses -optimal ligand selection & LiCl avoids deleterious transmetalation pubs.acs.org/doi/10.1021/ja…
Our work on Ni-Catalyzed Cross-Electrophile Coupling of Aryl Triflates with Alkyl Halides is now online at @J_A_C_S Congrats to Seoyoung, Matt, Ben, and Daniel! Check it out! doi.org/10.1021/jacs.4…
Welcome to Abi! We're excited to see all your awesome work in the group! 🥳✌️
Wondering "What is XEC"? Want to use XEC but don't know where to start? Check out our guide to XEC, which includes a flowchart comprised of all the data we compiled during the writing of our Chemical Reviews publication! weixgroup.chem.wisc.edu/xec-guide/
We're incredibly proud to say that our review of Cross-Electrophile Coupling: Principles, Methods, and Applications in Synthesis is now online and open access at @ACSChemRev! Congrats to the team for this labor of love (and data!) pubs.acs.org/doi/10.1021/ac…
Decarboxylative Cross-Coupling Enabled by Fe & Ni Metallaphotoredox Catalysis | JACS @UWMadisonChem @EmoryUniversity @EmoryChem @TotalSyntheses #Minisci #Decarboxylative #CrossCoupling #FeNi #Metalaalphotoredoc #Catalysis pubs.acs.org/doi/10.1021/ja…
pubs.acs.org
Decarboxylative Cross-Coupling Enabled by Fe and Ni Metallaphotoredox Catalysis
Decarboxylative cross-coupling of carboxylic acids and aryl halides has become a key transformation in organic synthesis to form C(sp2)–C(sp3) bonds. In this report, a base metal pairing between Fe...
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