Medicinal chemist @BioAscent | PDRA: Lawrence group @EdinburghUni | PhD: Aggarwal group @BristolUni | MChem: @UniStrathclyde | Creator of @NewInSynthesis
Hi all, I’ve recently started a weekly newsletter focused on highlighting key papers in organic synthesis that have been published in the previous week.
If you’re interested in reading more you can find the website linked below 👇
https://t.co/oolX1LF9fV
@RestIsPolitics@campbellclaret@RoryStewartUK MSD scrapped a £1B London R&D hub, cut 125 jobs & blasted the UK as “not internationally competitive” while AZ paused a £200M investment & scaled back a £450M expansion in the UK after Gov support faltered. Does the UK no longer value the life science sector or its scientists?
Do you struggle to keep up with the organic synthesis literature? Our former postdoc @SHBennett_ has started the Organic Synthesis Newsletter, a fantastic weekly summary of the recent literature. I highly recommend you subscribe for this FREE resource!!
https://t.co/n0nYq7SktX
Interested in the origins of stereoretentive enantioconvergence? @FrichardChem and I have just written a "Behind the Paper" post where we explain all - starting from @biomimetic_chem's 2012 (!) total synthesis of rac-incarvilleatone.
https://t.co/S1pVid0gYR
#OrganicChemistry
It was a privilege to work on such a beautifully designed project and a joy to come in everyday and work with such talented colleagues, all of whom worked so hard towards this outcome! Particular thanks go to my post-doc colleagues @FrichardChem@dJon_es@VDemertz!
Enantioconvergence with complete stereoretention.
Check out how @biomimetic_chem developed a new method for enantioconvergence and in one case joined two enantiomers of a racemate into an essentially single (99.99% e.e.) enantiomer using one branch of the methodology.
Issue #2 was just released this morning and I’ll put a link to that below but first I’d like to say thank you very much to all who have subscribed so far! I really appreciate the support and I hope this will be a useful resource going forward!
https://t.co/3LPEIgnpWf
Hi all, I’ve recently started a weekly newsletter focused on highlighting key papers in organic synthesis that have been published in the previous week.
If you’re interested in reading more you can find the website linked below 👇
https://t.co/oolX1LF9fV
The serendipitous discovery of a t-BuLi mediated dehalogenation-aromatization reaction enabled the total synthesis of Beraprost and set the stage for a unique approach to the modular synthesis of indolines. Congrats to the team who put so much into the project @SHBennett_
@willwh_@J_A_C_S Thanks Will! It was really cool to see that deuterium shift occuring, maybe even opens up the possibility for other non-H/D 1,2-shifts!
Great to see this out in @J_A_C_S! The serendipitous discovery of a t-BuLi mediated dehalogenation-aromatization reaction really facilitated the total synthesis of Beraprost and set the stage for a unique approach to the modular synthesis of indolines.
An unusual elimination reaction, via a carbene intermediate, enabled a novel aromatization process for the synthesis of indolenes and dihydrobenzofurans and paved the way for a short synthesis of beraprost. Congrats to the team. @BristolChem@SynthAtBris@J_A_C_S
Check out our new pre-print that shows you don’t need labile stereogenic units to achieve stereoconvergency! https://t.co/SQRSuOEGXr Stereoretentive-enantioconvergent reactions represent a new approach to #AsymmetricSynthesis.
#Chiral#Catalysis#Enantioconvergent
I had a great experience working with Andy and his group - the depth of knowledge and quality of chemistry there is incredible and I can’t recommend them enough.
I look forward to seeing what comes out of the group in the future and starting a new career @BioAscent!
Thank you for validating a cool procedure for aldol and dimerisation of succinaldehyde in very high ee. Very useful for prostaglandin synthesis and other 5-ring carbocycles. @DirkTrauner@SynthAtBris@Organicsynthes_