Symmetrical cleavage of disulphides is fast and biocompatible

A team of researchers led by Prof. Frank Glorius and Michael Teders from the University of Münster and by Prof. Dirk Guldi from the University of Erlangen-Nuremberg have presented a new chemical reaction path which may prove ...

'Click chemistry' reactions may boost cancer-fighting drug potency

Researchers at The Scripps Research Institute (TSRI) have developed a quick and easy way to simultaneously modify dozens of drugs or molecules to improve their disease-fighting properties. Using the approach, scientists exchanged ...

Chemists use modified DNA nucleotides to create new materials

DNA evolved to store genetic information, but in principle this special, chain-like molecule can also be adapted to make new materials. Chemists at The Scripps Research Institute (TSRI) have now published an important demonstration ...

Team presents new synthesis method for click chemistry

A recent study by researchers affiliated with UNIST has presented a new way to advance the click chemistry. This has applications in the synthetic chemistry of new drugs and the development of functional high molecules and ...

Click and declick of amine and thiol coupling reaction

(Phys.org)—A group of researchers from the University of Texas have developed a sequential, two-step amine and thiol coupling reaction via click chemistry using a derivative of Meldrum's acid. This reaction is reversible ...

A practical gel that simply 'clicks' for biomedical applications

If you opt to wear soft contact lenses, chances are you are using hydrogels on a daily basis. Made up of polymer chains that are able to absorb water, hydrogels used in contacts are flexible and allow oxygen to pass through ...

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