CATNIP for the win! Read our newest work with the Gomes group- doi.org/10.1038/s41586… Allie Paton, PhD Gabe Gomes Daniil Boiko Alison Narayan

Bit of a shot in the dark, but has anyone ever prepared this nifty Mitsunobu reagent using the 40% in tol. solns of DEAD instead of the pure reagent? (This feels like a Nick Chiappini 🏳️‍🌈 question)

Check out our latest article in J. Am. Chem. Soc.! We developed a new cascade reaction that combines alkylation, Heck carbopalladation, and C(sp3)–H annulation to generate cyclopropane or cyclobutane heterocycles. pubs.acs.org/doi/10.1021/ja…

Check out our latest work on generation of quaternary stereocenters through asymmetric oxy-Cope rearrangement! Out now in J Org Chem/Org Lett #OrgLett. Congratulations GANESH KARAN Susanta Bhunia Shubham Find out more on doi.org/10.1021/acs.or… IIT Kharagpur @Modhu Sudan Maji Anusandhan National Research Foundation

Pleased to share our Chemical Communications paper on the @totalsynthesis of Brevianamides X, Y & Z! 🌿A hydroxyproline-guided cascade reveals how oxidation timing directs X/Y divergence-bridging synthetic design and biosynthesis🌿. Congrats to all the authors! Link: pubs.rsc.org/en/content/art…

Happy to see the final version of this paper out! Congrats to Lauren Orr and Annika Page in our close collaboration with ⁦Toste Group⁩ and ⁦Novartis Science⁩ on second gen acyl silane photoaffinity handles for chemoproteomic applications! pubs.acs.org/doi/10.1021/ac…

Congratulations to team Ackerman-Biegasiewicz on their awesome new study entitled "Elucidation of Mononuclear Fe Photocatalysts for Visible Light-Induced Bond Homolysis (VLIH)" now available ChemRxiv! Super cool study! chemrxiv.org/engage/chemrxi…

Thrilled to share the first paper from our group at UCLA, online today in Science: “Biocatalytic, Asymmetric Radical Hydrogenation of Unactivated Alkenes” UCLA Chem & Biochem Science Magazine science.org/doi/10.1126/sc…

Congrats to Emilien, Maurus and Giorgia! Metal- and CO-Free Carbonylation of Alkyl Iodides J. Am. Chem. Soc.. pubs.acs.org/doi/abs/10.102…

#TotalSynthesis of Annotinolide B via Sequential Quinoline Dearomatization by Bhawyanth Duvvuru and Myles W. Smith at UTSW Media Relations in J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…

pubs.acs.org/doi/10.1021/ac…

Huge congratulations to the Ackerman-Biegasiewicz team on their work entitled "Harnessing Spectral Fingerprints to Predict Nickel Catalyst Performance"! LETS GO! chemrxiv.org/engage/chemrxi…

Excited to showcase my first first-author paper deposited on chemarxiv this morning! We propose using fundamental physical catalyst properties as features for ML prediction of nickel catalyst performance. Thanks to all those involved in this project. chemrxiv.org/engage/chemrxi…

Enantioselective #Synthesis of (+)-Auriculatol A by Jordan K. Thompson, Kala C. Youngblood, Yun Hao Shawn Teh, 乌鲁木齐, Zhehao Zhang, Scott C. Virgil, and Sarah E. Reisman at Caltech Chemistry & Chemical Engineering pubs.acs.org/doi/10.1021/ja…

Now online and open access: Article by Michael J. James & co-workers UoM Chemistry Reductive radical chain initiation through the thermal generation of carbon dioxide radical anion nature.com/articles/s4416…

Stereocontrolled #Synthesis of 8-Hydroxycurvularol, a Sesquiterpene with a Modified Trichothecene Skeleton by Johanna M. Masterson (Johanna Masterson) and Erik J. Sorensen (Sorensen Family) at Princeton Chemistry in J Org Chem/Org Lett pubs.acs.org/doi/10.1021/ac…

KFB Lab Alert: Our new chemoenzymatic strategy for isoxazoline synthesis through cryptic nitrile oxide formation is now available ChemRxiv! Huge congratulations to Manik Sharma for another awesome advance for the team! chemrxiv.org/engage/chemrxi…

♨️Hot of the Press! Our freshly brewed J. Am. Chem. Soc. on Redirecting Formate Delivery toward Alkenes is now live! Huge congratulations to Shantanu Nandi & Souvik Majumder 🥂 Indeed a great collaboration with Ignacio Funes-Ardoiz for DFT studies! Dorota Gryko 🔗Read here: doi.org/10.1021/jacs.5…

A Unified Synthetic Approach to 2-Alkyl Azetidines, Oxetanes, Thietanes and Cyclobutanes from Unactivated Alkenes | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/ja…