Markus Oppel makes supercomputers sweat, molecules dance in the light, and shows how a single sulphur atom can turn sunlight into a cell-damaging threat. Read the full story in our new blog, “We can bring any computer to its knees”: eurocc-austria.at/en/blog/we-c... #HPC #supercomputing
We were fascinated by the incredible Lewis Acid-Catalyzed Alkene-Aldehyde Coupling from @MaulideLab (pubs.acs.org/doi/full/10....) and couldn’t resist diving deeper into its mechanism! Check it out! @univie.ac.at chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
Computational Insights into the Mechanism of Lewis Acid‐Catalyzed Alkene‐Aldehyde Coupling
The Lewis acid-catalyzed coupling of alkenes and aldehydes presents a modern, versatile synthetic alternative to classical carbonyl addition chemistry, offering exceptional regio- and stereoselectivi...
chemistry-europe.onlinelibrary.wiley.com
Chemical reactions may seem like pure magic, but unraveling their mechanisms deepens the wonder! Feel the magic in our latest study! pubs.rsc.org/en/content/a...
Diastereoselective hydride transfer enables a synthesis of chiral 1,5-carboxamido-trifluoromethylcarbinols
The deployment of fluorinated functional groups has become a widespread tool in medicinal chemistry due to the impact of fluorine on lipophilicity and metabolic stability. Among these compounds, enant...
pubs.rsc.org
Optimizing geometries of complex intermediates and transition states can be quite a challenge, especially with large molecules—but we’re not afraid to tackle it! 😅 onlinelibrary.wiley.com/doi/10.1002/...
Enantioconvergent Negishi Cross‐Couplings of Racemic Secondary Organozinc Reagents to Access Privileged Scaffolds: A Combined Experimental and Theoretical Study
An enantioconvergent palladium-catalyzed Negishi cross-coupling of aryl electrophiles with racemic secondary organozinc reagents has been developed. This transformation enables access to enantioenric...
onlinelibrary.wiley.com
Calculations and experiments come together, creating a synergy that elevates our understanding of new reactions! Have you ever pondered the functionalization of polyols? We've got some news to share! @univie.ac.at onlinelibrary.wiley.com/doi/10.1002/...
https://onlinelibrary.wiley.com/doi/10.1002/anie.202315329
Wiley Online Library requires cookies for authentication and use of other site features; therefore, cookies must be enabled to browse the site. Detailed information on how Wiley uses cookies can be fo...
onlinelibrary.wiley.com
We've all heard of paracetamol, but have you ever wondered about its synthesis mechanism using organoselenium chemistry? Or considered the use of sulfur as an alternative? Explore our new study for answers! chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1...
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.202302386
Wiley Online Library requires cookies for authentication and use of other site features; therefore, cookies must be enabled to browse the site. Detailed information on how Wiley uses cookies can be fo...
chemistry-europe.onlinelibrary.wiley.com