C-H bonds, peptides, carbohydrates

Joined April 2018
We turned a triazole ring into a molecular mousetrap—snapping up amino groups for bioconjugation! 🧠💥 Super reactive, highly selective, and thiol-tolerant. Great teamwork with Huadong Xu (Changzhou University)!
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We’ve been dreaming of this type of conjugation chemistry for years—and finally, a simple fix to a stubborn problem, all thanks to just a tiny drop of CS₂. Minimalist chemistry is the new gold. ✨
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A huge thank you to our amazing guest editors, Masayuki Inoue, Lara Malins @Malins_lab, and Hans Renata @hanzyduzit, for organizing this OL special issue on radical-mediated reactions! Special thanks to Steve Ritter and Matt Saucier for your invaluable support.
Special Issue alert! 🚨 This one is truly •radical• pubs.acs.org/page/orlef7/vsi… This VSI highlights the state of the art in radical reaction development and the strategic incorporation of radical reactions in the construction and modification of important molecules.
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Interested in sulfonium ylide chemistry? Don’t miss Biao Xiong's latest Organic Letters paper @JOC_OL on a sleek Cu-catalyzed [3+2] route to 5-CF3-pyrroles, starting from CF3-imidoyl sulfonium ylides and terminal alkynes.
Copper-Mediated Cyclization Gives 5-Trifluoromethylpyrroles: Practical approach uses CF3-imidoyl sulfoxonium ylides and terminal alkynes chemistryviews.org/copper-me…
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HFIP's magic shines again, enabling peptide stapling with alpha-ketoaldehydes through unique imidazolium linkers, outperforming natural “glycation” processes. We proposed HFIP aggregates act as a proton shuttle for efficient deacylative C--C cleavage.
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We are grateful for the swift publication of this work in @NatureSynthesis and the outstanding editorial assistance received!
N-glycoside synthesis, a tough nut to crack, is now approachable with our new light/Cu catalysis method, allowing N-glycosidic bond formation under mild conditions with exceptional water tolerance and unique chemoselectivity. Another fruitful collaboration with MJ Koh @MJKoh87.
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N-glycoside synthesis, a tough nut to crack, is now approachable with our new light/Cu catalysis method, allowing N-glycosidic bond formation under mild conditions with exceptional water tolerance and unique chemoselectivity. Another fruitful collaboration with MJ Koh @MJKoh87.
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Two simple reagents, HCHO and hexafluoroisopropanol (HFIP), unleash new chemical magic! HCHO effectively “sucks” the alpha C-H bond from common alkyl amines in HFIP solvent, enabling hydride liberation without metals or light. It works for complex systems, too.
Formaldehyde-Mediated Hydride Liberation of Alkylamines for Intermolecular Reactions in Hexafluoroisopropanol @J_A_C_S #Chemistry #Chemed #Science pubs.acs.org/doi/10.1021/jac…
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I am deeply humbled and honored to be part of the editor team of Organic Letters. I very much look forward to serving the journal and our organic community☺️
We are thrilled to announce that Prof. Gong Chen of Nankai University will be joining #OrgLett as an Associate Editor on December 1. Known for his work on metal-catalyzed C-H functionalization and on peptides and oligosaccharides, Gong may soon be handling your manuscript!
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Learn more about #Asymmetric C–H Functionalization in our Thieme Web #Cheminar with Joanna Wencel-Delord (@DelordWencel), Shigeki Matsunaga, Nicolai Cramer, and Bing-Feng Shi (@bfshi). Chaired by Liu-Zhu Gong and Gong Chen (@GongChenLab). Register now 👉📝fal.cn/3onTo
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Gong Chen retweeted
Extendable stapling of unprotected peptides by crosslinking two amines with o-phthalaldehyde disq.us/t/44d05fd Our new chemistry for peptide macrocycles publishend on @NatureComms. Many thanks and Congrats @GongChenLab.
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Please check out this work if you are interested in C-glycoside synthesis. The next goal will be alkyl C-H glycosylation :)
Stereoselective Synthesis of C-Vinyl Glycosides via Palladium-Catalyzed C-H Glycosylation of Alkenes (Chen) onlinelibrary.wiley.com/doi/…
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Very excited to have our collobaration work with Sukbok Chang selected as the Synfact of the Month! Thank you @MarkLautens and @thiemechemistry
❇️ In this Synfact of the Month @MarkLautens and Joachim Loup highlighted the ✨Synthesis of Hydrazides by N–N Coupling ✨ reported by @GongChenLab from @NanKaiUniv 👏 👉 fal.cn/3gVJB
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Check out @gongchenlab, Xiaojie Lu et al.'s latest article 😍⬇️ Streamlined construction of peptide macrocycles via palladium-catalyzed intramolecular S-arylation in solution and on DNA 🔗 ow.ly/K5vm50E6bVZ
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Simple FeCl2 catalyst enables a very efficient method to make N-N bond. A great collaboration with Prof Sukbuk Chang #KAIST. Please check out our latest research on #nitrene chemistry, published in @NatureChemistry
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Our first study on DNA-encoded library synthesis. The Pd-catalyzed S-arylation chemistry is very effective and robust under biocompatible conditions. Many thanks to Xiaojie Lu at SIMM for a great collaboration! - now published in Chemical Science pubs.rsc.org/en/content/arti…
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Very proud of this chemistry 🤪
Cooperative Stapling of Native Peptides at Lysine and Tyrosine or Arginine with Formaldehyde (Chen) onlinelibrary.wiley.com/doi/…
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NEW in @ChemicalScience 📢 A Rapid and Sensitive Method for Chiroptical Sensing of α-Amino Acids via Click-like Labeling with o-Phthalaldehyde and p-Toluenethiol by @GongChenLab et al. Read it here for free! 🔗 ow.ly/vLUS50D28IW
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