When sulfur disappears without trace

August 17, 2018, University of Vienna
When sulfur disappears without trace
New selective synthesis of all 1,4-dicarbonyl isomers from sulfoxides and selected important bioactive compounds featuring the 1,4-dicarbonyl motif. Credit: © Maulide Group

Many natural products and drugs feature a so-called dicarbonyl motif— in certain cases, however, their preparation poses a challenge to organic chemists. In their most recent work, Nuno Maulide and his coworkers from the University of Vienna present a new route for these molecules. They use oxidized sulfur compounds, even though sulfur is not included in the final product. The results are now published in Science.

Organic chemists are constantly seeking new for novel drugs and materials. To synthesise molecules, they will analyse the functional groups present within the target and choose a suitable strategy accordingly. However, for some molecules, identifying a suitable strategy can be very challenging, for instance, when the distances between the functionalities in the molecule do not match the "natural" polarity of potential precursors.

One classical example is that where two carbon-oxygen double bonds (also called "carbonyl" groups) are separated by four carbon atoms. "These 1,4-dicarbonyl compounds are significantly more difficult to make than the corresponding 1,3- or 1,5-analogues, and this is something we teach every student in Organic Chemistry I at the University of Vienna," says Nuno Maulide, professor for organic synthesis at the Institute of Organic Chemistry of the University.

To make these motifs in the lab, no good strategy exists. "What we teach our students is that the polarity inversion of one of the reaction partners is required, but there is no really good solution to the problem," says Maulide. This is a severe problem, as 1,4-dicarbonyls are found in many , drug targets and several enzyme inhibitors used in pharmaceuticals.

Nuno Maulide and his coworkers from the Organic Chemistry Department of the University of Vienna have now developed a new synthetic route to these structures using reagents called sulfoxides, an oxidized species of sulfur. "What makes our method so fascinating is that sulfur is decisively involved in the reaction, but it doesn't even appear in the final molecule," explains Immo Klose, DOC-fellow of the Austrian Academy of Sciences and co-first author of the study. "This is also what makes this reaction intriguing, because it is not obvious at first sight how the starting materials form the product," said Klose. Indeed, during the reaction, sulfur leaves the reactive molecule in a so-called "traceless" manner, meaning it is not present in the final products.

Not only is the sulfoxide partner critical in the reaction, the researchers have shown that by choosing the right starting sulfoxide, each one out of four possible isomers of the product can be obtained selectively. "Our sulfoxide reagents have two positions that can be changed: the itself and the two carbons that are connected to it. This gives us four possible combinations," explains Dainis Kaldre, former Postdoc at the Institute of Organic Chemistry and co-first author. "The great thing is, by changing between these 4 possible combinations, we effectively fine-tune the into delivering selectively each of the four configurations of the final product that are possible," says Kaldre. This makes the method extremely general and powerful.

New drug molecules unlocked

"The flexibility of our method can now be used to make a breathtaking amount of molecules that were not even thinkable before," explains Maulide. The group has already shown this in the initial report in the journal Science, in which they demonstrate a simple way to make matrix metalloproteinase inhibitors. "There was no good way to make these compounds. In particular, it was very difficult to make a specific configuration in selective way; now, with our method, we can make any one out of the 4 possibilities, at will," says Maulide.

The reactive species with which the sulfoxides are combined are somewhat exotic intermediates called "vinyl cations."

"It is remarkable how basic research on 'exotic molecules' can so easily result in breakthroughs for society. This is a very welcome—and timely—reminder of the immense value that lies in investing in basic research," so Maulide concluding.

Explore further: An environmentally friendly chemical reaction that does not waste any atoms

More information: "Stereodivergent synthesis of 1,4-dicarbonyls by traceless charge–accelerated sulfonium rearrangement" Science (2018). science.sciencemag.org/cgi/doi … 1126/science.aat5883

Related Stories

Chemists build new chemical structures on unreactive bonds

July 28, 2017

Making complicated organic molecules is like solving a Rubik's cube. Organic chemists need to design sequences of reactions to carefully build up parts of a molecule, while maintaining the structure at other sites. Although ...

Precise deuteration using heavy water

June 6, 2018

NUS chemists have developed a more effective method using heavy water splitting to swap hydrogen atoms on organic molecules with their heavier cousins (deuterium) for pharmaceutical applications.

Creating complex molecules in just a few steps

March 7, 2018

Researchers have found a way to convert single bonds between carbon and hydrogen atoms in a chemical molecule into carbon-carbon bonds. This so-called C-H activation is considered a promising strategy for producing complex ...

Recommended for you

Fish-inspired material changes color using nanocolumns

March 20, 2019

Inspired by the flashing colors of the neon tetra fish, researchers have developed a technique for changing the color of a material by manipulating the orientation of nanostructured columns in the material.

0 comments

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more

Click here to reset your password.
Sign in to get notified via email when new comments are made.