Cross-Electrophile Coupling to Form Sterically Hindered C(sp2)–C(sp3) Bonds: Ni and Co Afford Complementary Reactivity | Journal of the American Chemical Society UW–Madison UW-Madison Chemistry Weix Group Total Synthesis and Methodology Highlights pubs.acs.org/doi/10.1021/ja…

Efficient Preparation of Chiral Hydroxylamines via Nickel-Catalyzed Asymmetric Hydrogenation of Oximes Bowen Li, Jianzhong Chen, and Wanbin Zhang orgsyn.org/demo.aspx?prep…

Photoinduced PhI(OAc)2-Mediated Cross-Dehydrogenative Heteroarylation of Aldehydes. pubs.acs.org/doi/abs/10.102…

Interested in strained rings or fluorine for medicinal chemistry - check out Hikaru’s work on divergent synthesis of difluorocyclobutanes, on ChemRxiv: doi.org/10.26434/chemr…

Our second work on the synthesis of N-CF3 compounds now out in Nat. Commun.. No column chromatography needed! rdcu.be/enPhW

Photo- and Copper-Catalyzed Enantioselective Oxidation of Benzylic C(sp3)–H Bonds | Journal of the American Chemical Society Total Synthesis and Methodology Highlights pubs.acs.org/doi/10.1021/ja…

Direct Deoxyboration of Alkyl Alcohols | Organic Letters pubs.acs.org/doi/10.1021/ac…

Efficient Aminations of Aryl Halides by a Cu(II) Catalyst | Journal of the American Chemical Society College of Chemistry UC Berkeley Total Synthesis and Methodology Highlights pubs.acs.org/doi/10.1021/ja…

HKU has reached an unprecedented milestone, climbing to 11th place in the 2026 #QS World University Rankings QS World University Rankings. This achievement marks the second consecutive year of record-breaking, following its rise to 17th globally in 2025. HKU has also solidified its position

Catalytic Asymmetric Synthesis of Axially Chiral Methylenecyclopropanes | Journal of the American Chemical Society Uyeda Lab Research at Purdue Purdue University Total Synthesis and Methodology Highlights pubs.acs.org/doi/10.1021/ja…

Our latest cobalt catalysis paper is out now in JACS ASAP! See Jaysan, Deepesh, Vibha, and Mingxin’s work on asymmetric methylenecyclopropanation below! 🧪 pubs.acs.org/doi/10.1021/ja…

Universal Reagent for Mild and Stereospecific Nucleophilic Substitution of Alcohols with Amines doi.org/10.1002/anie.2…

Gram-Scale #TotalSynthesis of Illisimonin A by Liangchao Zhu, Jinrui Li, and Zhaohong Lu in J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…

#TotalSynthesis of Daphenylline via Diels–Alder Cycloaddition and Rhodium-Catalyzed C–H Alkynylation by Wei Chen, Aohang Liu, Jinwei Huang, Pengfei Yu, Huaxuan Zhang, Huilin Li, Xingang Xie, Gaoyuan Zhao, and Xuegong She in J Org Chem/Org Lett pubs.acs.org/doi/10.1021/ac…

Synthesis of Borylated Orphaned Cyclopropanes through a Boron-Enabled Cycloisomerization Reaction | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/ja…

Skeletal editing of pyrrolidines by nitrogen-atom insertion | Science science.org/doi/10.1126/sc…

Debabrata Maiti and the DM Lab IIT Bombay team unveil a C(sp²)–C(sp³) cross-electrophile coupling platform for aryl chlorides enabled by newly developed ligands #AngewandteVIP • onlinelibrary.wiley.com/doi/10.1002/an…

Check out this new review from our team - spot on our mission to reimagine synthetic Organic Chemistry exploiting technology 👇

Our latest paper out in J. Am. Chem. Soc. Catalytic Asymmetric Ionic Hydrogenation of α-Alkyl Styrenes pubs.acs.org/doi/10.1021/ja…