
Sherburn Lab
@sherburn_lab
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The Sherburn Research Group are a Synthetic Organic Chemistry research group based at the Research School of Chemistry, Australian National University.
Australian Capital Territory
Joined November 2017
RT @kurtilaszlo: The second day of lectures (October 4, 2024) at ASTS-NDM 2024 ( will feature @MortenMeldal & K.C.….
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RT @kurtilaszlo: The first day of lectures (October 3, 2024) at ASTS-NDM 2024 ( will feature @FeringaLab & K.B. Sha….
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RT @kurtilaszlo: On behalf of the Organizing Committee, I am delighted to announce that the inaugural symposium "The Art and Science of Tot….
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RT @maddie_sowden: Super stoked to announce that I will be joining Auburn University @AuburnU as an Assistant Professor in the fall! Shouto….
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RT @Jones_Research: Corrected proof of this one from Jeremy and co. has now appeared in @ChemEurJ. It is now open access and has picked up….
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Fundamental hydrocarbons and low oxidation state main group chemistry, together at last! Our first paper from an exciting new collab with the illustrious @Jones_Research, just accepted @ChemEurJ Congratulations to everyone involved @ANUChemistry @ChemistryMonash.
Jeremy's work, and first fun collab with @sherburn_lab (ANU), on the Mg(I) redn of [4]dendralenes and related oligo-alkenes (inc. Mg(I) mediated assembly of a diene, CO, and H2 to a triolate!) has been accepted @ChemEurJ. #ozchem @ChemistryMonash
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RT @OChem_Grenning: #ORPGRC 2024 chaired by @Humulonimbus & I now has the preliminary list of academic speakers posted! . .
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RT @ChemistryViews: Cadiot–Chodkiewicz Reactions Made Air-Tolerant:.Ascorbate as a reductant suppresses unwanted side reactions. https://t.c….
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A breath of fresh air for cross-couplings! Borrowing from both Click and ARGET-ATRP methodologies, we report air tolerant Cadiot-Chodkiewicz and Sonogashira couplings with ascorbate, now in #OrgLett @JOC_OL. Congrats to Alfred and Maddie @ANUChemistry.
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Solve your synthesis malaise with amazing azas! Heterobicycles in one shot from dendralenes, out now in #OrgLett @JOC_OL. Congrats to Yi-Min and Jose @ANUChemistry Another fun collab with important comp insights from Joseph and Michelle
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Reagent-free, catalyst-free, strain-activation free C–C bond formation! 😉 Check out our latest contribution in @J_A_C_S Another fun collaboration with the Coote group. Congratulations to Zhipeng, Nick, Maddie and Rhys. @ANUChemistry
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What do you prefer? The synthesis of dendralenes or dendralenes in total synthesis? 🤔 Don’t worry: you we have both covered. Check out our two publications in the latest issue of @J_A_C_S out today! @ANUChemistry
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Thanks to Nancy McGuire @J_A_C_S for Spotlighting our recent [4]dendralene paper! @ANUChemistry @scienceANU.
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RT @NatureSynthesis: In this week's #NSynthPick we highlight the total synthesis of matrine alkaloids by @MagannNicholas @erinwestley @madd….
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@ANUChemistry @J_A_C_S . congratulations also to Erik, whose original work inspired the development of this approach, and who performed the first site-selective Diels-Alder reactions.
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Thanks to incredible work from Yi-Min, Maddie and Nick @ANUChemistry virtually any [4]dendralene or related polyene can now be made. Our latest paper on catalysis, synthetic methods and hydrocarbon chemistry is out today in @J_A_C_S. Congratulations all!
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Out now @J_A_C_S is our total synthesis of matrine alkaloids, featuring a [3]dendralene and a 2-fold intramolecular Diels-Alder strategy. Congratulations to Nick, Erin and Maddie: your resilience and perseverance are awe inspiring. @ANUChemistry
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