idw – Informationsdienst Wissenschaft
Nachrichten, Termine, Experten
Nachrichten, Termine, Experten
idw - Informationsdienst
Wissenschaft
A team led by Prof. Armido Studer from the University of Münster has introduced a strategy for converting carbon-nitrogen atom pairs in a frequently used ring-shaped compound into carbon-carbon atom pairs. The method has potential in the quest for active ingredients for new drugs, for example. The results are published in “Nature Chemistry”
In the field of chemistry, so-called skeletal editing is seen as a method suitable for changing ring-shaped structures precisely by swapping individual atoms. A team of researchers led by Prof. Armido Studer from the Institute of Organic Chemistry at the University of Münster has now introduced a new strategy for converting carbon-nitrogen atom pairs in pyridines – a ring-shaped compound frequently used as a synthesis building block – into carbon-carbon atom pairs. The method has potential in the quest for new drugs and materials which are often based on such molecule rings.
While the ring structure remains intact in the so-called peripheral functionalisation of rings – which involves for example the attachment of groups of atoms – skeletal editing requires the cleavage of robust bonds between carbon atoms or between a carbon atom and another atom within the ring. “In organic synthesis,” says Armido Studer, “this is considered to be particularly challenging – we can imagine it as a kind of surgical procedure.” Up to now, no synthesis strategy was known which could be used to swap complex pyridines by means of skeletal editing. In this new approach, the team produced benzenes and naphthalenes with functional groups which are attached precisely to specific positions. Functional groups are groups of atoms which play a decisive role in the properties of a compound.
“The pyridines which we used are inherently inert, making it difficult to modify them,” explains post-doc Dr. Qiang Cheng. “We first had to change their specific bonding structure – carrying out so-called dearomatization – in order to obtain significantly more reactive intermediates. The subsequent cycloaddition and rearomatization processes ultimately result in the formation of the skeletal-edited compounds.”
Debkanta Bhattacharya, a PhD student in Armido Studer’s team, adds: “Now, by using a so-called one-pot procedure, we can introduce synthetically valuable and medically significant functional groups to specific positions on rings.” Chemists speak of a one-pot reaction to describe a synthesis in which the reagents needed react with one another in a single vessel. The reaction sequence’s mechanism was theoretically analysed by Dr. Christian Mück-Lichtenfeld from the Institute of Organic Chemistry.
Prof. Armido Studer
University of Münster
Organisch-Chemisches Institut
Mail: studer@uni-muenster.de
Qiang Cheng, Debkanta Bhattacharya, Malte Haring, Hui Cao, Christian Mück-Lichtenfeld and Armido Studer (2024): Skeletal editing of pyridines through atom-pair swap from CN to CC. Nature Chemistry; DOI: https://doi.org/10.1038/s41557-023-01428-2
Criteria of this press release:
Journalists, Scientists and scholars
Chemistry
transregional, national
Research results, Scientific Publications
English
You can combine search terms with and, or and/or not, e.g. Philo not logy.
You can use brackets to separate combinations from each other, e.g. (Philo not logy) or (Psycho and logy).
Coherent groups of words will be located as complete phrases if you put them into quotation marks, e.g. “Federal Republic of Germany”.
You can also use the advanced search without entering search terms. It will then follow the criteria you have selected (e.g. country or subject area).
If you have not selected any criteria in a given category, the entire category will be searched (e.g. all subject areas or all countries).
