Transforming Boron Chemistry By Exploring Boryl Radical Reactivity
This project aims to innovate organic chemistry by developing novel catalysis using boryl radicals for efficient C–B bond formation and new synthetic methods for complex molecules.
Projectdetails
Introduction
Our ability to construct organic molecules is central to the wellbeing of our society. Boron-containing compounds are some of the most used tools to aid this. These materials are used as building blocks when “stitching” molecules together and also as catalysts in many different settings. The invention of innovative strategies to prepare and exploit borylated molecules is integral to discovering and manufacturing many products that we use daily.
Project Aim
The overarching aim of this proposal is to innovate organic chemistry by inventing novel catalysis concepts based on the reactivity of boryl radicals, an underutilized class of reactive intermediates. My group has introduced a novel approach to generate these species from amine-borane precursors and here I aim to:
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Establish a general platform to borylate aromatics using boryl radicals. This blueprint for C–B bond formation will introduce amine-borane functionalities instead of standard boronic acids/esters. This will provide unprecedented synthetic capacity because the amine-borane will serve a dual role acting first as a directing group for ortho/meta functionalization and then as a cross-coupling handle.
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Explore boryl radicals in innovative cascade reactions leading to the divergent assembly of sp3-rich fragments. These methods will expedite the preparation of poly-functionalized materials, tapping into unexplored areas of chemical space.
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Establish boryl radicals as “H-atom transfer” catalysts to achieve the “philicity umpolung” of nucleophilic radicals. This concept will introduce unprecedented retrosynthetic tactics and enable the merge of boryl radical reactivity with asymmetric organocatalysis.
Conclusion
Overall, this cohesive and innovative research plan offers the unique opportunity to discover novel and exciting transformations that go far beyond what is currently possible. Achieving this project will provide unprecedented tools for the preparation and use of borylated materials in synthesis and catalysis.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.999.250 |
Totale projectbegroting | € 1.999.250 |
Tijdlijn
Startdatum | 1-1-2024 |
Einddatum | 31-12-2028 |
Subsidiejaar | 2024 |
Partners & Locaties
Projectpartners
- RHEINISCH-WESTFAELISCHE TECHNISCHE HOCHSCHULE AACHENpenvoerder
Land(en)
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This project aims to explore reversible diradical formation in donor-acceptor organic molecules to enhance light-emitting materials and drug discovery through novel design criteria.
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C-HANCE aims to revolutionize C–H functionalisation by utilizing charge control to enable novel reactions and broaden substrate applicability, enhancing synthetic chemistry and downstream applications.
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