organic chemistry, photo-triggered processes, DNA-templated synthesis, looking for TT for 2027!!

New York, NY
Joined April 2012
Dr. Reg So retweeted
Two distant stereocentres. One smooth catalytic cycle! Our latest @JACS installs 1,6-stereocentres via Ir-cat asymmetric allylation of resorcinol boronate complex, enabling the total synthesis of merocyclophane A. Congrats, team! 🔗 doi.org/10.1021/jacs.6c14045 @BristolChem
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Check out this Perspective in #JMedChem: gem-dimethylcarbinol can be considered as a tert-butyl bioisostere. Add C(CH3)2OH to your list of favorite bioisosteres! go.acs.org/ePz
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Dr. Reg So retweeted
In @J_A_C_S, we show the extension of our nitrate-reduction-based diazotization strategy to aliphatic amines! Consecutive nitrate reduction by substoichiometric hydroquinone is key and enables in-situ diazotization followed by (pseudo)halogenation! 🔓 tinyurl.com/36es3e3f
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Proud to present our newest new-to-nature #enzyme activity, primary amination of aromatic feedstocks using simple hydroxylamine. @caltechCCE #directedevolution
New in @ACSCentSci! 🧪 We engineered biocatalysts that selectively install primary amines onto aromatic feedstocks using hydroxylamine as the nitrogen source. Huge thanks to my co-authors: @CaseyAtTheVat, Ethan Lin, @Yueming_Long_ @francesarnold doi.org/10.1021/acscentsci.6…
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Dr. Reg So retweeted
The last work of Stefano Nicolai, Daphne Lucidarme and Matthew Wodrich on the formal cycloaddition of azadienes and bicyclobutanes is now accepted in Chemical Science! doi.org/10.1039/D6SC05550H
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Deprotonation and visible-light excitation generate a highly reducing excited state capable of activating strong C–Hal bonds. Congrats to Alex and @IndrajitGhosh85 Acridone Anion as a Highly Reducing Visible-Light Photocatalyst doi.org/10.1039/D6CC05207J
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From stoichiometric donor–acceptor assemblies to catalytic turnover: what makes EDA complex catalysis work? Check out our latest review in Angewandte Chemie, exploring the design principles and mechanistic requirements of EDA complex catalysis.✨✨ doi.org/10.1002/anie.1736780
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Are you looking for a sustainable way to synthesize heterocycles ? ♻️ Check our latest @ACSChemRev on hetero-photocycloaddtions (HPCs) 💡 🫴shorturl.at/tBH0D Congrats to all the authors on this work ! 🎉 #Photochemistry #OrganicChemistry
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Dr. Reg So retweeted
Our sixth Account on CH activation focus on transient covalent approach to boost metal substrate affinity: from the discovery of L,-X TDG to total synthesis. pubs.acs.org/a/5448172?guest…
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A collection on the last 26 years of works on photo heterocycloadditions. 🫴pubs.acs.org/chreay/article/… Hope the community will find it useful! Huge congrats to @CristianRosso92 @sara_cuahuetes @Er_Goti @VascoCorti @e_marcantonio95
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Dr. Reg So retweeted
🚨After 5y in making, unveiling a special discovery🌌in @Chem_CP: Cross-coupling transient(vinyl/sp!) radicals.🚫Ni/Fe/radical sorting/hydrazides.✅Covalent-rotating organoPC💡dyads template 2 precursors, generate& cross-couple radicals in close proximity tinyurl.com/mtkd45p4
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Now online: Modular synthesis of 3,3-diaryloxetanes go.​nature.​com/4dmzRak 🧪
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Dr. Reg So retweeted
This is a fascinating Nobel Prize, and congratulations to the winners. I would be remiss, however, not to acknowledge Donna Blackmond’s mechanistic brilliance and her substantial contributions to our understanding of this chemistry.
Kenso Soai – awarded the 2026 #NobelPrize in Chemistry – designed the first chemical reaction in which only one of the potential mirror images was formed. Other than life itself, no one had ever achieved this feat. The Soai reaction is one of the most spectacular chemical experiments ever conducted.
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