Meanwell Lab

@ASHOK4NOBLE To clarify, only the technician position is restricted to Canadians/PRs. The PDF position can be visa sponsored.

@Meanwell_Lab Hello Dr. Michael Meanwell, I am ASHOK POLU, Postdoc at Department of Radiology, University of Pittsburgh, Pennsylvania, USA. Will you consider my application with visa sponsorship if possible? Please let me know since you already mentioned priorities for Canadian or PR .

We are also looking to hire a technician (small molecule purification) to start as soon as possible #ChemTwitter. Email meanwell@ualberta.ca with your CV. Only Canadian citizens and PRs will be considered for this position.

We are currently hiring for a postdoc position (organic synthesis) to start as soon as possible #ChemPostdoc #ChemTwitter. Email meanwell@ualberta.ca with your CV and research summary. Only successful candidates will be contacted.

We are proud of lab members @Subhojit_JU_UoA (left) and @DinithiGR (right) for both winning an Alberta Graduate Excellence Scholarship (AGES). Congrats Jit and Dinithi! Keep up the great work! @ualbertachem

Our lab @ualbertachem has 2 PhD positions open for Fall 2026 in catalysis and synthetic organic chemistry. Contact me via email if interested!

Check out our lab's most recent work led by @Subhojit_JU_UoA on electrochemical deutero-carboxylation at rdcu.be/eONMS.

We are currently looking for a postdoc (organic synthesis) to start winter 2026 or sooner @Meanwell_Lab #ChemPostdoc #ChemTwitter. Email meanwell@ualberta.ca with your CV and research summary. Only successful candidates will be contacted.

@That_Chemist Many thanks Joey for this generous highlight of our work

Ever seen the Meanwell Nucleoside synthesis? I discuss this, and other useful transformations of acetals in this installment of Important Papers: Useful Transformations of Ketals & Acetals (Important Papers) youtu.be/U55vm0GfIsw

@DakeGaurav Thanks Gaurav!

@Meanwell_Lab Congratulations Soumik, Rohit and Dr. Meanwell💐

Check out our most recent work on chemoselective electrochemical birch carboxylation of pyridines - now published in Green Chemistry pubs.rsc.org/en/content/art…

@g_laudadio Thanks Gabriele :)

@Meanwell_Lab Congrats to the team! Beautiful work :)

The X-Chem Research Excellence Award is presented to a scientist who has made a distinguished contribution to medicinally relevant organic or biophysical chemistry in Canada. Congrats to Matthew Macauley of @UAlberta on being the recipient of this award. buff.ly/4fYmgV8

Exciting news for prospective graduate students! We will host your visit to Edmonton and our department during our visiting weekend on Mar 7-8, 2025 (free trip for those eligible!). For eligibility and registration, visit our website at: forms.gle/ro7hAcesjFJtf3…

We are hosting an online information session about the chemistry graduate programs at the University of Alberta @11:30am MT on Jan 20th. Sign up here: docs.google.com/forms/d/12-pls…

Thank you to Global News Edmonton @GlobalEdmonton for covering our work on developing better ways to make nucleoside analogues. Check out the story here: bit.ly/3DnRGGz

@ualbertaScience Thank you for highlighting our work

𝗥𝗲𝘀𝗲𝗮𝗿𝗰𝗵𝗲𝗿𝘀 𝗱𝗲𝘃𝗶𝘀𝗲 𝗮 𝗾𝘂𝗶𝗰𝗸𝗲𝗿, 𝗺𝗼𝗿𝗲 𝗲𝗳𝗳𝗶𝗰𝗶𝗲𝗻𝘁 𝘄𝗮𝘆 𝘁𝗼 𝗺𝗮𝗸𝗲 𝗹𝗶𝗳𝗲-𝘀𝗮𝘃𝗶𝗻𝗴 𝗺𝗼𝗹𝗲𝗰𝘂𝗹𝗲𝘀 Improved method for creating nucleoside analogues opens the door to discovering countless treatments for everything from cancer to viral diseases. A team of researchers has found a quicker and more efficient way to create nucleoside analogues, a type of small molecule that can be used in treatments for everything from cancer to viral diseases. “Nucleoside analogues are among the most important molecules to the advancement of modern medicine,” says Michael Meanwell, assistant professor in the Department of Chemistry and corresponding author of a paper published in Nature Communications describing the new process. bit.ly/4eX6h9e #UAlberta #Science #Research #Chemistry #MedicalResearch

We are currently looking for a postdoc (organic synthesis) to start spring 2025 or sooner @Meanwell_Lab #ChemPostdoc #ChemTwitter. Email meanwell@ualberta.ca if interested.

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 requisite catalysts) or potentiostats for electrochemistry. Now, such transformations can be accomplished with the same ease that one conducts a Suzuki coupling. You can scale up (its homogeneous) or scale down (use cheap parallel screening plates). Moisture is tolerated and base metal catalysis is used. As the best engineers like to say, "The best part is no part". Now, chemists have the option to remove the redox part from radical couplings. Quick Summary: Sulfonyl hydrazides are disclosed as versatile radical precursors as exemplified with seven new C–C bond forming, redox-neutral cross-couplings with: (1) activated olefins, (2) alkyl halides, (3) redox active esters, (4) aryl halides, (5) alkenyl halides, (6) alkynyl halides, and (7) a trifluoromethylating reagent to forge C(sp3)-C(sp3), C(sp3)-C(sp2), and C(sp3)-C(sp) bonds. Sulfonyl hydrazides are stable and usually crystalline substances that can be accessed in a variety of ways including transiently from hydrazones to achieve a net reductive arylation of carbonyl compounds. Exogenous redox (chemical, photo/electrochemical) additives are not necessary as these functional groups serve the dual role of radical precursor and electron donor. The operational simplicity (homogeneous, water tolerant, dump-and-stir) and practicality of the method are demonstrated as well as applications to streamlining synthesis and mild late-stage functionalization.

🚨Our chemistry department @ualbertachem will be hosting a virtual information session for prospective international students about our graduate programs (MSc +PhD) on Nov 13th (8:00am MT). To sign up and for more information check out the link below. docs.google.com/forms/d/e/1FAI…