Accessing pharmacophoric space via asymmetric protonation

Lead Research Organisation: University of St Andrews
Department Name: Chemistry

Abstract

Asymmetric catalysis has revolutionized the way molecules are made and are essential to the continued production of myriad products from small bioactive molecules to materials and from small scale to manufacture. A number of these processes have become privileged, with their impact demonstrated from tonne-scale application to the Nobel Prize. Increased mechanistic understanding of catalytic reactions underpins improvements of existing processes while driving development of new methods. By interrogating reactivity and selectivity in a newly described reaction, this proposal aims to bring new understanding to the underpinning catalytic processes while providing methods for the preparation of novel and synthetically powerful architectures.

Our preliminary studies using asymmetric protonation have recently been published and provide a solid foundation for the proposed work.
A series of additional supporting proof-of-concept experiments in support of this proposal have also given strong confidence in being able to deliver upon the objectives and aims of this proposal.

This proposal will comprehensively investigate this asymmetric protonation platform to allow predictability and the rational application of this chemistry as a method for the generation of scaffolds tailored towards application in Medicinal Chemistry, with specific applications within Chemical Development in collaboration with our industrial project partner.

Planned Impact

Potential Economic Impact of the Research. Catalysis is central to the preparation of molecules for healthcare (pharmaceuticals, imaging), food security (herbicides, pesticides), and devices and energy conversion/harvesting (materials, catalysts). The importance of catalysis and a strong UK presence in this field has been highlighted in major reviews including the International Review of Chemistry, REF, the RSC Chemistry Roadmap, and the Chemistry Innovation Knowledge Transfer Network roadmap. This National Importance is reflected in EPSRC physical sciences strategy: advances in catalysis support the Energy, Manufacturing the Future, and Healthcare Technologies themes and the "Dial-a-Molecule" Grand Challenge.

Underpinning this proposed research programme is the development of new knowledge within asymmetric catalysis. The new knowledge gained here may be used to facilitate more rapid access to molecules (e.g., in discovery phase) or more efficient access to molecules (e.g., in process chemistry) ultimately leading to economic gain of the company and wider UK in due course. In collaboration with Britol-Myer Squibb, as well as using our own established platforms, we will explore the application of this new synthetic methodology in the context of Medicinal Chemistry for the step-efficient construction of bioactive molecules with specific function. The applicant has strong programme of catalytic reaction development and collaborative Medicinal Chemistry projects with well-defined knowledge transfer mechanisms. The applied aspects have been designed in consultation with our project partner to ensure business relevance, therefore promoting impact and fostering further collaboration.

Outputs: Patent protection of intellectual property; exploration of licenses, develop new medicinal agents independently and in collaboration with Bristol-Myers Squibb.

Mechanisms of delivering Economic Impact: Knowledge Exchange partnership and EPSRC Impact Acceleration Account (IAA), Scottish Enterprise Proof of Concept or the Technology Strategy Board's Biomedical Catalyst. AJBW is a member of the CRITICAT CDT management team. Through CRITICAT we will be able to foster further industrial engagement that may lead to larger and wider impact.


Potential Societal Impact of the Research. The objective of this research is to improve knowledge and control of catalytic processes and show this can be applied. In the context of new knowledge, improved understanding of catalytic methods may allow the refinement of chemical processes that ultimately benefit the production of materials of products that may have a downstream impact on the consumer while also improving economy (see above). In the context of Medicinal Chemistry, new medicinal chemistry agents for hard to treat diseases (for example, the PI's programme targets Idiopathic Pulmonary Fibrosis, which has been granted Orphan Status) have a clear impact on society by prolonging or improving life. Thus the potential societal impact of this proposed programme could be very significant.

Outputs: Public discussion of the role of catalysis in the pharmaceutical industry; dissemination of results through the mainstream press, and UoS websites.

Mechanisms of delivering Societal Impact: Delivery of presentations at the Glasgow Science Festival and Glasgow Science Centre events. Public engagement activities as part of the CRITICAT CDT programme.
 
Description New fundamental information on the mechanism of reactions and new ways to make complex molecules
Exploitation Route The fundamental knowledge is immediately transferable to other processes and the methods to make complex molecules will be of utility to academic and industrial practitioners
Sectors Chemicals,Pharmaceuticals and Medical Biotechnology

URL https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202200060
 
Title Dataset underpinning "An alternative synthesis of cycloalkyl-substituted CPA catalysts and application in asymmetric protonation reactions" 
Description This is the raw data underpinning the above titled manuscript. 
Type Of Material Database/Collection of data 
Year Produced 2021 
Provided To Others? Yes  
URL https://risweb.st-andrews.ac.uk/portal/en/datasets/dataset-underpinning-an-alternative-synthesis-of-...
 
Title Dataset underpinning "Asymmetric synthesis of heterocyclic chloroamines and aziridines by enantioselective protonation of catalytically generated enamines" 
Description  
Type Of Material Database/Collection of data 
Year Produced 2022 
Provided To Others? Yes  
URL https://risweb.st-andrews.ac.uk/portal/en/datasets/dataset-underpinning-asymmetric-synthesis-of-hete...