2018 – WEIX RESEARCH GROUP

Multimetallic Ni- and Pd-Catalyzed Cross-Electrophile Coupling To Form Highly Substituted 1,3-Dienes

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Congrats to Julianna for receiving an Outstanding Chemistry Teaching Assistant Award for your work with Chem 636 and the NMR facilities! Well deserved! 🎉
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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.! @pubs.acs.org Congrats to Tianrui, Anthony, Kasturi, and our collaborators Madeline (@kozlowskigroup.bsky.social) and @novartis.bsky.social http://doi.org/10.1021/jacs.4c16912
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Our work on in-situ generation of alkyl chlorides using Ghosez’s reagent and coupling with aryl chlorides is now online at Org. Lett. Congrats Ben! @pubs.acs.org Check it out! doi.org/10.1021/acs.orglett.4c04676 #chemsky
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Our work on Ni-Catalyzed Cross-Electrophile Coupling of Aryl Triflates with Alkyl Halides is now online at JACS @pubs.acs.org. Congrats to Seoyoung, Matt, Ben, and Daniel! doi.org/10.1021/jacs.4c14769 https://doi.org/10.1021/jacs.4c14769
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Welcome to Abi! We're excited to see all your awesome work in the group! 🥳✌️
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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 Chem Rev! Congrats to the team for this labor of love (and data!) https://pubs.acs.org/doi/10.1021/acs.chemrev.4c00524