Tom D'Arcy
@tomddarcy
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Happy to be able to share my first publication, out now in @angew_chem. Find out how we used an unusual class of organocatalyst to prepare a bacterial metabolite, and a natural diterpenoid from simple phenols! @TotalSynthesis
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@Chiba_Group @ChemRxiv @PrattGroup Congrats guys, loved this, one of the best papers I’ve read in a long while!
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RT @BRBuckley: Please share! Last couple of days to apply for the Organic Chem POst-doc position in my lab! #chempostdoc
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@KUhokie42 We found some in our lab this week that had 10-30 mg/L using testing strips, it’s surprising
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RT @BRBuckley: 2yr Post-Doc position on asymmetric catalysis available in my group please rt! @lborouniversity @LeverhulmeTrust #chempostdo…
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RT @RiccardoDiSanza: 📢 FREE WEBINAR 📢 As part of our @SygnatureDiscov Guest Lecture series (#SGL) @JacobsenLab will talk about: "Privileged…
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@SM_IITJ @sudhir859 @RupashriDash @LisaRoyChem @JOC_OL @serbonline @CSIR_IND Congrats! Seems like a much nicer alternative to using Ni and a halo uracil. Does it work with normal (non-aza) uracils too? Apologies if it’s discussed in the manuscript, I don’t have access
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RT @BRBuckley: Delighted to receive @LeverhulmeTrust project grant funding to investigate asymmetric hydroxylative dearomatisation chemist…
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@sasha_sundstrom I’m thinking something that looks like a ‘carbonylative Larock’ - oxidative addition of the Ar-I and CO insertion, followed by Carbopalladation of the alkyne, coordination of the pyridine N, then reductive elimination
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RT @angew_chem: Organocatalytic Enantioselective Synthesis of Bicyclo[2.2.2]octenones via Oxaziridinium Catalysed ortho-Hydroxylative Pheno…
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@tom_armstrong Don’t think so mate but might have a look, supposed to be going to an SCI one in may
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