Jonathan Clayden retweeted
Super excited that our work on the rational design of 310-helical bundles is now out in @Nature! Congrats Prasun @dgr8ashoka for this impressive piece you have led in collaboration with @ClaydenGroup and @DiamondLightSou!
You can read it here: nature.com/articles/s41586-0…
Marina Hyde's always good value but she's brilliantly on fire today. theguardian.com/commentisfre…
Well done to Matthew Wootten for working out how to use a simple idea to create complex conformational behaviour in mixtures of chiral acids, bases, and a metal.
Our latest Pick of the Week is on molecular communication💬, by @JonathanClayden from @BristolChem! The @ClaydenGroup demonstrate communication of a conformational response to a spatially remote site 🔥. Read this #ChemSciPicks article for free: 🔗 doi.org/10.1039/D1SC06812A
Jonathan Clayden retweeted
Triarylmethanes and their Medium-Ring Analogues by Unactivated Truce-Smiles Rearrangement of Benzanilides @ClaydenGroup #openaccess onlinelibrary.wiley.com/doi/…
Some good news from the ERC arrived in my in-box last week :-) bristol.ac.uk/news/2020/marc…
Jonathan Clayden retweeted
With sadness, we are remembering our colleague Dr Stuart Warren who died yesterday. See our story about him here: ow.ly/qPsG50ySSI9
Jonathan Clayden retweeted
Alkylation of amino acids has resulted in active pharmaceuticals and building blocks for unnatual peptides. Now a general route for the equivalent arylation is reported in Nature. go.nature.com/2E8yldu
Jonathan Clayden retweeted
From @JonathanClayden ‘s group and we totally should have done tagging in the ‘official’ tweet. *shakes fist at Official Nature’s much bigger reach than mine*
Alkylation of amino acids has resulted in active pharmaceuticals and building blocks for unnatual peptides. Now a general route for the equivalent arylation is reported in Nature. go.nature.com/2E8yldu
Jonathan Clayden retweeted
A new way to modify amino acids, useful for synthesizing new medicine molecules. “This work allowed us to turn what was a scientific curiosity into (something) really practical" Jonathan Clayden, ERC grantee @BristolUni describes his discovery: bristol.ac.uk/chemistry/news… #EUfunded
Jonathan Clayden retweeted
Modification of amino acids provides new starting point for development of medical treatments - latest research from @JonathanClayden group published in @NatureNews nature.com/articles/s41586-0…
Jonathan Clayden retweeted
Extremely proud of our work from @JonathanClayden group on the asymmetric α-arylation of amino acids published in @nature disq.us/t/36wfp4s
Just out! At last a way to introduce (almost) any aromatic ring to the central C atom of (nearly almost) any amino acid, making either mirror image product at will: Asymmetric α-arylation of amino acids disq.us/t/36wfp4s
‘Natural substances’ and a natural woman | Brief letters theguardian.com/music/2018/a…
The latest method from the Clayden Group: move over Pictet and Spengler...!
Consecutive Ring Expansion and Contraction for the Synthesis of 1‐Aryl Tetrahydroisoquinolines and Tetrahydrobenzazepines - Angew Chem Int Ed onlinelibrary.wiley.com/doi/…
Jonathan Clayden retweeted
Spring has sprung in the @JonathanClayden group! pubs.acs.org/doi/10.1021/jac…
Collaborations with GSK can inspire all sorts of publications: theguardian.com/music/2017/d…
Jonathan Clayden retweeted
Medium-Sized-Ring Analogues of Dibenzodiazepines by a Conformationally Induced Smiles #RingExpansion (Clayden) doi.wiley.com/10.1002/anie.2…
Our membrane-bound synthetic receptor - just out in @NatureChemistry
rdcu.be/pQ7T
A tendril perversion (that kink in the telephone cable on your desk) trapped inside a helical molecule. dx.doi.org/10.1039/C6SC05474…
Our new way of making medium (8-12 membered) benzo-fused N heterocycles by a ring-expanding aryl shift. xitter.cf/angew_chem/status/7560…
Medium-ring nitrogen #heterocycles through migratory ring expansion #OrganicSynthesis @jonathanclayden doi.org/f3qqhq




















