Congratulations Ahmed and the team!!!

I’m excited to share our latest review with lovelockresearchgroup "Modern approaches to therapeutic oligonucleotide manufacturing " appearing today in Science Magazine

Excited to share our work on “Enantiocontrolled Azetidine Library Synthesis via Strain Release Functionalization of 1-Azabicyclobutanes” that appeared in ChemRxiv today. A great collaboration between Baran Lab and the Cravatt lab. Hayden Sharma

I’m happy to share our work on “An Improved P(V) Oligonucleotide Synthesis Platform” that appeared in ChemRxiv today. A great collaboration between Baran Lab, Elsie Therapeutic, and Hongene.

“Thymidine Phosphodiester Chemiluminescent Probe for Sensitive and Selective Detection of Ectonucleotide Pyrophosphatase 1”. Inspiring collaboration with Baran Lab, Appearing today in ChemRxiv: chemrxiv.org/engage/chemrxi…

Out now in Angewandte Chemie : onlinelibrary.wiley.com/doi/10.1002/an…

I’m happy to share our work on “Electrifying P(V): Access to Polar and Radical Reactivity” which appeared in ChemRxiv today.

Thrilled to share our new preprint in ChemRxiv, in which we unveil a new avenue to access valuable scaffolds for drug development that were previously virtually inaccessible. Huge thanks to all our collaborators for making this work possible!

Finally, RADICAL CROSS COUPLING without the exogenous REDOX. We disclose in ChemRxiv (chemrxiv.org/engage/chemrxi…) a broadly general platform for achieving transformations that normally required excess metallic or chemical reducing agents or photochemical setups (and their

Very exciting to disclose the remarkable reactivity of hydrazide in nickel-catalyzed cross-coupling. The reaction conditions are very simple—only nickel, ligand, a base, and solvent. The reaction proceeds rapidly, and the TLC results are super clean. Handling this radical

Final version published today in Angewandte Chemie : onlinelibrary.wiley.com/doi/epdf/10.10…

Electrifying P(V): Access to Polar and Radical Reactivity (Phil S. Baran and co-workers) Baran Lab • onlinelibrary.wiley.com/doi/10.1002/an…

Excited to share this work profiling a new P(V)-electrophile using our stereoprobe platform, where we discover a first-in-class, cell-active inhibitor of integral membrane protein TLCD1 and ID critical catalytic residues! Great collab w/Baran Lab biorxiv.org/content/10.110…

🚨RADICAL RETHINK: STEREORETENTIVE CROSS COUPLING UNLOCKED🚨 Today in ChemRxiv (chemrxiv.org/engage/chemrxi…) the first method for stereoretentive radical cross-coupling is disclosed. No fancy ligands or redox needed—just a Ni-diazene twist. 120 years after Gomberg, a new chapter

Join Tamara E and me at the IKA booth at #ACSSanDiego next week! Don't miss our presentations—see you there!

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Excited to share my first preprint as an independent PI! appeared today on ChemRxiv. We report a simple and practical route to 2,5-disubstituted thiazoles from N-substituted α-amino acids. A versatile method with broad scope. Check it out: [chemrxiv.org/engage/chemrxi…] #NewPI

Our latest paper is now out in J. Am. Chem. Soc. ! We unveil a new strategy to access elusive free oxoboranes—highly reactive species—via bridged boranoanthracenes and aromatization-driven extrusion. Congratulations to the team! pubs.acs.org/doi/10.1021/ja…

Final version out today in J. Am. Chem. Soc. : pubs.acs.org/doi/full/10.10…

We are proud to present our work on something really special, appeared in ChemRxiv today. We unlocked the synthetic application of DMF distonic radical anion with electrochemistry! Interested in the full story? See below! (1/n) chemrxiv.org/engage/chemrxi…