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📝Hot from press Nature Chemistry (🧵) Aromaticity is not a constraint when arenes participate in dipolar cycloaddition. Yes, aromaticity breaks at low temperatures with high efficiency! Congratulations Shubhangi Aggarwal, Alex, Dmitry Eremin and Rudra doi.org/10.1038/s41557… 1/4

HEY Y'ALL! Do you remember a few #MechanismMonday(s) ago when I couldn't tell you the answer because it was unpublished work?! Well! Here it is in print! BIG BIG congrats to my friends Fokin Lab USC (Shubhangi Aggarwal and Dmitry Eremin) and the team! Kick ass work. (:

Can we expand the reactive chemical space by involving aromatic rings in synthesis? 🧐 Overjoyed to witness my graduate work find its home Nature Chemistry. Thank you team Fokin Lab USC USC Chemistry USC Bridge Institute 🎉 nature.com/articles/s4155…

Excellent paper... I have also enjoyed looking the pictures of the final products 😍. Congratulations to the team!! A very comprehensive and thorough piece of work... Well deserved🔥

Fokin Lab USC Not only was the chemistry from this Fokin Lab USC Nature Chemistry paper amazing, as you point out, the SI is astounding! Seriously, I’ve never enjoyed looking through an SI so much!

An exciting development in expanding accessible drug-like chemical space with new structurally rich chemotypes via new click-like chemistry! Congratulations Fokin Lab USC ! #drugdiscovery

Dear #ChemTwitter, we are now in the process of forming a Synthesis Workshop Editorial Board to make this initiative more sustainable in the long run and continue to become more community-based. Check below for more details! RTs highly appreciated!!

Good morning, Houston! Come to my poster TP267 #ASMS267 to see what microdroplet chemistry has to offer for selective oxidation reactions Fokin Lab USC USC Chemistry

Our June issue went live last week with a very pretty cover highlighting research from Fokin Lab USC nature.com/nchem/volumes/…

Congratulations Dr. Shubhangi Aggarwal on defending today USC Chemistry! Bittersweet day in Fokin Lab today! Good luck in your future endeavors Bristol Myers Squibb process. So proud of you! #proudPI USC Bridge Institute

Befriending commonly perceived foe-air💨 for the synthesis of organic molecules by channelizing the unique reactivity of captodative radicals a.k.a push-pull radicals‼️ Delighted to share another piece of my dissertation published J. Am. Chem. Soc.! 👩‍🔬 pubs.acs.org/doi/full/10.10… Fokin Lab USC

Generation and Aerobic Oxidation of Azavinyl Captodative Radicals | Journal of the American Chemical Society USC Chemistry USC #Aerobic #Oxidation #Azavinyl #Captodative #Radicals pubs.acs.org/doi/10.1021/ja…

The latest issue of JACS is live! On the cover this week: Authors Fokin Lab USC describe a cascade reaction that selectively incorporates oxygen into the carbon−carbon backbone of alkynes using air as the source. Read the article here ➡️ go.acs.org/6Vr

Delighted to see the final version of this collaborative study out in Angewandte Chemie, describing a robust & scalable e-chem ⚡️ method to Ni(0) w/ #BMSChemistry Baran Lab Julien Vantourout. Thx to our fearless leader CamilleR! tinyurl.com/mr2yyy8a

Selecting an amide bond coupling reagent? Choose safely! #BMSChemistry’s David George, Michael Williams, and Greg Beutner show that TCFH is a safer reagent for various transformations… and many times higher yielding!! onlinelibrary.wiley.com/doi/10.1002/hl…

I am beyond thrilled to share our group's first independent contribution as a preprint. We discovered an iron-catalyzed cross-electrophile coupling and used it for disulfide bioconjugation, drug synthesis, and other applications! Find the preprint here: chemrxiv.org/engage/chemrxi…

Need to set some stereocenters? Check out the latest from #BMSChemistry on this Asymmetric Transfer Hydrogenation! Great work by Seung Wook and the rest of the team pubs.acs.org/doi/10.1021/ac…

It was really great to be a part of the BMS-organized symposium at the ACS GCE Conference (Atlanta, GA) this year!! I'm excited to continue sharing the work we are developing at #USC!

Fun fact of the day: Suzuki reactions don’t have to be aqueous! Especially when it enables an efficient telescoped process! Excited to share my favourite process from an awesome and collaborative #BMSChemistry team. pubs.acs.org/doi/10.1021/ac…