Radical and Radical-Polar Crossover Logic in Terpenoid Synthesis
This project aims to redefine terpenoid biogenesis by demonstrating the interplay of radical and polar reactivity, enabling sustainable synthesis of druggable natural products for medical applications.
Projectdetails
Introduction
The synthesis of complex natural products has shaped the field of organic chemistry, with translational applications spreading further into medicinal, agrochemical, and material sciences. As the largest class of natural products, terpenoids play a variety of roles in mediating antagonistic and beneficial interactions macroscopically, i.e., among organisms, and microscopically, i.e., on a (sub)cellular level.
Role of Terpenoids
They defend many species of plants, animals, and microorganisms against predators, pathogens, and competitors, and they are involved in conveying messages within these organisms.
Challenges in Synthesis
Facilitating and streamlining access to the most complex terpenoids, heavily rearranged and highly oxidized triterpenoids, requires an understanding of Nature’s ways to biosynthesize these structures, i.e., of their biogenesis. Biomimetic synthesis can only then provide routes that outrival classical retrosynthetic planning. In the absence of a plausible biogenesis proposal, this strategy is not accessible, though.
Current Paradigm
So far, biogenesis proposals have, in lieu of validated intermediates and enzymes, followed the paradigm of polar mechanisms and evoked standard textbook reactions involving ionic intermediates to account for skeletal rearrangements.
Project Aim
The aim of this project is to disprove this paradigm and cross this perceived limit of reactivity. Thus, we will provide chemical proof that terpenoid biogenesis is not sufficiently explained by polar mechanisms, but rather is an intricate interplay of radical and polar reactivity.
Crossing Boundaries
The border we attempt to cross is the one between two very different chemical entities: radicals and ions.
Development of New Strategies
Development of radical-polar crossover logic will evolve robust and selective routes to access druggable triterpenoid natural products modulating the immune system, targeting cancer, and combating pathogens.
Added Value
Added value comes from the involvement of modern photoredox catalysis strategies to initiate radical-polar crossover cascades in a sustainable fashion.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.987.059 |
Totale projectbegroting | € 1.987.059 |
Tijdlijn
Startdatum | 1-5-2022 |
Einddatum | 30-4-2027 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- GOTTFRIED WILHELM LEIBNIZ UNIVERSITAET HANNOVERpenvoerder
Land(en)
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