Molecular Assembly Triple Click Chemistry: A New Approach to Building Complex Molecules with Precision

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Scientists at Tokyo University of Science have developed stable trivalent platforms for triple click chemistry, making it easier to synthesize complex molecules with high precision. This method allows for efficient and selective formation of highly functional triazoles, with potential applications in drug development, material science, and bioengineering.

Middle molecules with a molecular weight of more than 1,000 are difficult to synthesize due to multiple steps and time-consuming nature, demanding the development of a new approach that can overcome these disadvantages. Click chemistry has become an essential tool in applied chemistry due to its simplicity, efficiency, and versatility. This approach to chemical synthesis allows for quick and reliable joining of small molecules into larger, more complex structures, often with minimal side reactions and byproducts. By definition, click chemistry reactions are highly selective and efficient, making them ideal for creating specific compounds in a controlled and predictable manner.

By taking this idea two steps further, chemists have been developing molecular platforms that allow for triple click chemistry — the development of stable molecules with three different functional groups that serve as distinct, targetable reaction sites. Although these “trivalent” platforms enable the efficient synthesis of complex compounds, the selective formation of triazoles using platforms with azide and alkyne moieties remains an unsolved challenge.

Against this backdrop, a research team led by Associate Professor Suguru Yoshida from Tokyo University of Science (TUS), Japan, set out to develop novel trivalent platforms capable of producing highly functional triazoles.

The researchers succeeded in creating stable trivalent platforms for triple click chemistry, thanks to a longer linker in the central scaffold. The research team demonstrated how a wide variety of molecules could be produced by sequentially targeting each functional moiety in the trivalent platform. For example, they leveraged the sulfur–fluoride exchange reaction to target the fluorosulfonyl moiety and produce different alcohols in high yields without affecting the azide and alkyne moieties. Then, they performed diverse transformations on the azide moiety, including hallmarks like copper-catalyzed azide–alkyne cycloaddition, strain-promoted azide-alkyne cycloaddition, and Bertozzi–Staudinger ligation. Finally, through a broad range of possible third transformations targeting the remaining alkyne moiety, the researchers successfully synthesized complex triazoles.

Notably, it was not strictly necessary to follow the order described above when targeting each moiety, as the researchers demonstrated triazole formations selectively in subsequent experiments. On top of this, complex triazoles could be obtained in a straightforward, one-pot reaction. “Selective click reactions with molecules that have both azide and alkyne moieties are not easy, but we were able to elucidate that each click reaction proceeds in a highly selective manner by properly choosing alkyne or azide reaction partners that react preferentially with the targeted group under the suitable conditions,” explains Yoshida.

The triple click chemistry platforms developed in this study have important implications in several applied fields. For example, functionalized multi-triazoles, which can be readily prepared in high yield, are valuable in drug development, material science, and bioengineering. They are compatible with many biological targets, such as enzymes and receptors, indicating potential pharmaceutical applications. The bio-active middle molecules synthesized via triple click chemistry can help in recovering from intractable diseases. Moreover, they are important in catalysis and materials development, serving as the basis for the design of polymers, sensors, coatings, and coordination frameworks.

“Our ultimate goal is to create new molecules that will revolutionize life sciences, and we conceived this research as a method for assembling simple component molecules all at once,” concludes Yoshida. “The proposed method enables the simple synthesis of multifunctional molecules and a wide variety of medium-sized molecules, and we expect it to be widely useful in pharmaceutical science, medicinal chemistry, chemical biology, and materials chemistry.”

The proposed approach utilizes simple initial materials rather than complex materials, promoting sustainable pharmaceutical synthesis. Additionally, the time-saving aspect of this approach can speed up the research process. Overall, the efficient trivalent platform molecules presented in this study will help accelerate progress toward more sustainable chemistry, hopefully leading to green synthesis protocols, better medical treatments, and environmental and agricultural advancements.

Reference: Three-step click assembly using trivalent platforms bearing azido, ethynyl, and fluorosulfonyl groups; Chemical Communications; DOI: 10.1039/D4CC06585A

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