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Congratulations Dr. Lauren Ehehalt on a fantastic thesis defense! We're so excited to see all your future work at Eastman Chemical Co.! 🥳🎉🎓
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Our work on the translation of Nickel-Catalyzed C(sp2)–C(sp3) Cross-Electrophile Coupling to Non-Amide Solvents is now online in Org. Lett.! @pubs.acs.org Congrats to Brett, Julianna, Michelle, and wonderful collaborators at @novartis.bsky.social Check it out! doi.org/10.1021/acs.orglett.5c01011 https://doi.org/10.1021/acs.orglett.5c01011
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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

Member Type

DiBenedetto, Tarah

Parsons, née Olivares, Dr. Astrid

Melchor, Zulema

Wotal, Dr. Alexander

Zhao, Dr. Yang

Rugg, née Dorn, Dr. Stephanie

Hilferding, Keith

Diao, Lingbo

Chen, Sylvia

Prinsell, Dr. Michael