A team of researchers from KU Leuven, in
Belgium, has developed a chemical reaction that yields fully functional
1,2,3-triazoles.
Triazoles are chemical compounds that can
be used as building blocks for more complex chemical compounds,
including pharmaceutical drugs.
Leveraging the compound's
surprisingly stable structure, drug developers have successfully used
1,2,3-triazoles as building blocks in various anti-HIV, anti-cancer and
anti-bacterial drugs.
But efforts to synthesise the compound
have been hampered by one serious hurdle: they depend on harmful heavy
metals to work, and this severely limits their biological applications.
In
new experiments, a research team at KU Leuven's Molecular Design and
Synthesis lab confirm for the first time that 1,2,3-triazoles can be
synthesised through a metal-free, three-component reaction using readily
available ingredients.
"We were able to develop a reaction that
provided a good yield, high regioselectivity and easy access to
diversely functionalised 1,2,3-triazoles," said corresponding author Wim
Dehaen.
"In other words, the reaction produces plenty of the
compounds we're looking for, does so reliably without unwanted or
unexpected outcomes, and does this in a way that makes it easy for us to
isolate the compound. This makes our method highly desirable," said
Dehaen.
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