A postdoctoral position, funded by the @LeverhulmeTrust for up to 36 months, is available to join my group @EdinburghChem. The project focuses on biomimetic approaches to natural product synthesis.
Deadline: 28th August 2025.
https://t.co/S5GelmP6Cv
A postdoctoral position, funded by the @LeverhulmeTrust for up to 36 months, is available to join my group @EdinburghChem . The project focuses on biomimetic approaches to natural product synthesis.
Deadline: 18th April 2025.
https://t.co/tT7iRFgml9
Looking for your first step towards an independent career? We offer a 3-year-independent fellowship to support postdoc researchers from backgrounds under-represented in chemistry (e.g., women, minority ethnic, LGBTQI+, disabled, low-income backgrounds) https://t.co/r786dBKMi1
IT'S FINALLY HERE! Starting October 28th, the Synthesis Workshop Advanced Organic Chemistry course will begin releases through our regular YouTube channel for FREE, thanks to the massive efforts of presenters from many researchers from academia and industry!
Support by sharing!
German photographer Herlinde Koelbl asked past Nobel laureates to draw the essence of their award-winning research on the palm of their hand. Thank you, @francesarnold, for talking to me about being one of her subjects. On @forbes --> https://t.co/OUvywKOSYQ
Check out some of our team's work towards releasing boryl-caged organophosphates using hydrogen peroxide! What we've learned from this work has inspired a couple fun new projects and collaborations for #Teamboron in the @floreanciggroup!
Iterating on sulfur fluoride exchange, K. Barry Sharpless and @HarborSpring have introduced phosphorus fluoride exchange for building complex products from a central phosphorus hub. ‘Just one step to the left and the world is different,’ says Sharpless.
https://t.co/j4kVuh6wOd
Hey PUI researchers, do you qualify to publish in @JOC_OL with free open access? If your institution has the All ACS Package and you are the submitting corresponding author, yes you do. Learn more here https://t.co/XnZFPTaaK3. We look forward to your next submission.
#ChemTwitter, the #GrenningLab is actively recruiting a postdoc! Gain mentoring experience with an amazing group of Grad/UG students! Help develop enantioselective, "energetically challenging" Cope rearrangements! Enjoy the vibrant #CollegeTownLife in Sunny @Gainesville! #PlzRT!!
compound 25 - Merck | https://t.co/AFrPnu7Omx
This case study of- lead optimization incorporates a “bow-tie” spirocyclopropyl group and a flipped indazole as a non-classical C-H hinge binder to improve PK properties in targeting LRRK2 for Parkinson’s disease.
While there are lots of options to beat water with H-bond acceptors, for H-bond donors its not so easy. Here's a analysis of the nice dataset in Schwöbel et al. You can see that CH-donors essentially never beat water. In the NH donor class, amides usually beat water but 1/4
@JSpencerlab I took that on an iPhone 12. No filters or anything, Scotland is just stunning! I’m back in my home uni in Florida now. I spent last year in Dundee while doing a sabbatical with @ADS_StAndrews! I hope you enjoy your trip, Dundee is a great city!
🧲 This is a real #NMRchallenge for students and #NMR geeks developed by the NMR group @IOCBPrague: practice solving structures from hundreds of NMR spectra and become an NMR guru.
https://t.co/roY6xZUtY0
Mind-blowing work from Carl Mansson & Noah Burns out today in JACS — aqueous CuSO4 catalyzes light-promoted [2+2] Kochi–Salomon cycloaddition of simple olefins. The response from everyone I've shown this to is the same: disbelief, then delight.
https://t.co/GtyiwigJVF