Joe Woods
@jfwoods.bsky.social
Self-assembled materials
Postdoc in the Wennemers Group, ETHZ
PhD in the Rickhaus Group, UZH
Postdoc in the Wennemers Group, ETHZ
PhD in the Rickhaus Group, UZH
Great start to the week with our latest carpyridine findings out in @jacs.acspublications.org! Water and carpys now self-assemble together, forming linear stacks as revealed by micro-ED. Check it out: doi.org/10.1021/jacs...
@michelrickhaus.bsky.social @avj-chem.bsky.social @rickhauslab.bsky.social
@michelrickhaus.bsky.social @avj-chem.bsky.social @rickhauslab.bsky.social
A Supramolecular Nanosheet Assembled from Carpyridines and Water
The use of water as a solvent to facilitate supramolecular self-assembly and polymerization is well-documented; however, it is rare that water acts as a monomer that undergoes polymerization. We repor...
doi.org
May 19, 2025 at 4:48 PM
Great start to the week with our latest carpyridine findings out in @jacs.acspublications.org! Water and carpys now self-assemble together, forming linear stacks as revealed by micro-ED. Check it out: doi.org/10.1021/jacs...
@michelrickhaus.bsky.social @avj-chem.bsky.social @rickhauslab.bsky.social
@michelrickhaus.bsky.social @avj-chem.bsky.social @rickhauslab.bsky.social
Reposted by Joe Woods
🚨 New preprint from our group! We report a photocatalytic, regiodivergent method to functionalize saturated N-heterocycles at the α- or β-position. The metal-free reaction runs in water with a flavin catalyst and gives rapid access to sought-after piperidines. Check it out here: 🔗 tin.al/DqxU
May 7, 2025 at 1:22 PM
🚨 New preprint from our group! We report a photocatalytic, regiodivergent method to functionalize saturated N-heterocycles at the α- or β-position. The metal-free reaction runs in water with a flavin catalyst and gives rapid access to sought-after piperidines. Check it out here: 🔗 tin.al/DqxU
Reposted by Joe Woods
🚨 Happy to share a new preprint – our group’s first!
🔗 chemrxiv.org/engage/chemr...
We report a novel synthetic method to access cyclic ethers from diketones, powered by simple borane catalysts.
Thanks to the whole team for their excellent work!
🔗 chemrxiv.org/engage/chemr...
We report a novel synthetic method to access cyclic ethers from diketones, powered by simple borane catalysts.
Thanks to the whole team for their excellent work!
April 30, 2025 at 3:55 PM
🚨 Happy to share a new preprint – our group’s first!
🔗 chemrxiv.org/engage/chemr...
We report a novel synthetic method to access cyclic ethers from diketones, powered by simple borane catalysts.
Thanks to the whole team for their excellent work!
🔗 chemrxiv.org/engage/chemr...
We report a novel synthetic method to access cyclic ethers from diketones, powered by simple borane catalysts.
Thanks to the whole team for their excellent work!