Seung Hwan CHO
@shchom83
POSTECH, South Korea
Eid Mubarak! We are happy to share our latest work @JOC_OL on Programmable Strategies for the Conversion of Aldehydes to Unsymmetrical (Deuterated) Diarylmethanes and Diarylketones | Organic Letters pubs.acs.org/doi/10.1021/ac… Congrats to @vipingavit8 ,Nicole , @NadimEghbarieh
This week's Paper-of-the-Week (POW) presentations in our weekly group meeting featured some great work by @SandfordLab +@pfizer, @shchom83, @bobbypaton + @YuyangDong and Wu + Zhu group! #Chemistry #Boron
[1,3]-Hydride Shift in α-Boryl Cations: Strategic Design of Fluorine-Triggered Cyclopropanation | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/ja…
Thrilled to share our collaborative work with Prof. Yoonsu Park’s group published in Nature Communications: Superacid counteranion as flexible-coordinating ligand for asymmetric organo-bismuth catalysis. Congratulations to Jin Hyun and Seok Yeol! doi.org/10.1038/s41467…
🌪️🔥🌊🌍 Mastering all four? We did it with alkenes! Our @Nature paper with @bobbypaton lab reveals a modular boron-mediated strategy solving the long-standing challenge of accessing tetrasubstituted alkenes with full stereo-control. Congrats team! nature.com/articles/s4158…
organic-chemistry.org/abstracts/lit7… The combination of copper(I) bromide and H8-BINOL derived phosphoramidite ligand catalyzes an enatiotopic-group-selective allylation of gem-diborylalkanes with allyl bromides.
1,1-Diborylalkanes as Versatile Precursors for Copper-Catalyzed Diastereo- and Enantioselective Allylic Substitution (@thiemechemistry): thieme-connect.com/products/ejour… (@shchom83).
🎉 Proud moment! Our Main Group team just published their 2nd paper in @JACS_Au! They uncovered how O₂ activation mechanisms differ across P, Sb, and Bi - pushing the boundaries of main group chemistry 🧪 Read more: pubs.acs.org/doi/10.1021/ja…
beilstein-journals.org/bjoc/articles/… Editor's pick: Recent advances in #allylation of chiral secondary #alkylcopper species. By Seung Hwan Cho @shchom83 @CPostech, Jun Hee Lee @DG_univ, et al. Published diamond open access 💎🔓 in #BJOC. Thanks to all authors + guest editors + referees 🏅
Cantonese cuisine with Prof. Ito @haj19932469 and Prof. Cho @shchom83 on Hong Kong island
Our group photo in 2025 although we couldn't enjoy cherry blossom much due to cold weather.
Regiodivergent Alkylation of Pyridines: Alkyllithium Clusters Direct Chemical Reactivity | Journal of the American Chemical Society @kaistpr @KAIST_Chem @postech2020 @IBS_media @TotalSyntheses pubs.acs.org/doi/10.1021/ja…
.@usualmoney went from $0 to $1.8B TVL in under 6 months. Lately, it’s been steady around $1.18B–$1.2B, generating revenue, all of which goes to $USUAL stakers ( $USUALx holders). I believe it will climb again soon, they have interesting features about to launch. I’m breaking…
Interesting to discover that organozinc reagents react with inversion of configuration with pi-allyl iridum complexes, unlike other electrophiles where they react with retention. Congratulations to Hong Cheng for his meticulous studies. @J_A_C_S @BristolChem @AggarwalLab
Iridium-Catalyzed Stereocontrolled C(sp3)–C(sp3) Cross-Coupling of Boronic Esters and Allylic Carbonates Enabled by Boron-to-Zinc Transmetalation | Journal of the American Chemical Society @BristolUni @BristolChem @VarinderAggar11 @TotalSyntheses pubs.acs.org/doi/10.1021/ja…
Air & Thermally Stable Cyclic (Alkyl)(amino)carbene Ru Complexes: Efficient Ring Expansion Metathesis Polymerization | JACS @SeoulNatlUni @postech2020 @ETH_en @ETH_Materials @EunsungLee5 - New Ru catalysts with tethered carbenes -pubs.acs.org/doi/10.1021/ja…
Please check out our new achievement in Boron chemistry: Size-Programmable Matteson-Type Annulation: Construction of Spirocycles from Simple Cyclic Ketones | ChemRxiv - go.shr.lc/3VJMEKT
Thrilled to share my first postdoc paper in ACS Catalysis, exploring allyl–allyl coupling and chirality pairing! Stereospecific and Stereodivergent Allyl–Allyl Coupling: Construction of Vicinal Tertiary and All-Carbon Quaternary Stereocenters pubs.acs.org/doi/10.1021/ac…
Copper-Catalyzed Regio-, Diastereo-, and Enantioselective Allylic Alkylation with 1,1-Diborylalkanes | Journal of the American Chemical Society @TotalSyntheses #Cu #Catalysis #Regio #DiastereoSelective #Enantioselective #Allylic #Alkylation #DiborylAlkanes pubs.acs.org/doi/10.1021/ja…