Grant: Alliance Grants
Université d'Ottawa
$58,000.00
Overcoming and embracing oxidation for the synthesis of bioactive molecules
FY 2024-25
Summary
Synthetic organic chemistry lies at the center of the pharmaceutical industry's efforts to invent and prepare the next generation of life-saving drugs. As the diversity, predictability, and robustness of well-established chemical reactions grows each, so to does the amount of chemical space that gets searched for medicinally-relevant molecules. The continued success of global drug discovery efforts is thus closely tied to research in organic chemistry methodology. This proposal seeks to develop next-generation chemical transformations that have been identified by the industrial partners as being of high-value and allow them to access molecular scaffolds that have been previously unexplored by their medicinal chemistry teams due to lack of reliable and efficient methods. Oxidation plays a central role throughout. Molecular oxygen in the atmosphere is essential for life, facilitating aerobic oxidation that fuels the body. However, in most chemical reactions carried out in the pharmaceutical industry, aerobic oxidation is a difficult-to-control side reaction that hinders productive synthesis. Even with stringent efforts to exclude oxygen, oxidative degradation of substrates and catalysts can be difficult to avoid. However, in some cases, oxidation can also be embraced as a productive strategy by which valuable new transformations can be realized. This proposal targets both of these issues. For cross-coupling reactions that generate new C-C and C-N bonds, the inclusion of anti-oxidant additives will be explored with the anticipated benefit of expanding the applicability of these transformations to those that may previously have been hindered such as couplings with sensitive sulfur, oxygen, or boron-containing functional groups. Towards harnessing oxidation, the transient oxidation of amines to hydroxylamines will be exploited to develop new stoichiometric and catalytic C-N bond forming reactions via hydroamination pathways, providing a new way to access saturated nitrogen-containing heterocycles. Applications of these methods to access novel molecular space for the discovery of new drugs will be carried out in close collaboration with industrial partners who have previously struggled with these challenges in redox chemistry.
Program
Alliance Grants
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
576253-2022
Name nom
Newman, Stephen SG
Department département
Chemistry
Organization id
28
Institution établissement
Université d'Ottawa
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2024
Competition year année de concours
2022
Award amount
58000
Program id
ALLRP
Program name en
Alliance Grants
Program name fr
Subventions Alliance
Group en
RESEARCH PARTNERSHIPS
Group fr
PARTENARIATS DE RECHERCHE
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
504
Area of application group en
Manufacturing processes and products
Area of application group fr
Procédés et produits industriels
Area of application en
Human pharmaceuticals
Area of application fr
Produits pharmaceutiques administrables à l'homme
Research subject code
3703
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Organic syntheses
Research subject fr
Synthèses organiques
Field of research list names en
Not available
Field of research list names fr
Non disponible
Socioeconomic objective list names en
Not available
Socioeconomic objective list names fr
Non disponible
Application title
Overcoming and embracing oxidation for the synthesis of bioactive molecules
Keywords
amines; asymmetric catalysis; cross-coupling reactions; free radicals; nickel; organic synthesis; oxidation; palladium; transition metal catalysis
Application summary
Synthetic organic chemistry lies at the center of the pharmaceutical industry's efforts to invent and prepare the next generation of life-saving drugs. As the diversity, predictability, and robustness of well-established chemical reactions grows each, so to does the amount of chemical space that gets searched for medicinally-relevant molecules. The continued success of global drug discovery efforts is thus closely tied to research in organic chemistry methodology. This proposal seeks to develop next-generation chemical transformations that have been identified by the industrial partners as being of high-value and allow them to access molecular scaffolds that have been previously unexplored by their medicinal chemistry teams due to lack of reliable and efficient methods. Oxidation plays a central role throughout. Molecular oxygen in the atmosphere is essential for life, facilitating aerobic oxidation that fuels the body. However, in most chemical reactions carried out in the pharmaceutical industry, aerobic oxidation is a difficult-to-control side reaction that hinders productive synthesis. Even with stringent efforts to exclude oxygen, oxidative degradation of substrates and catalysts can be difficult to avoid. However, in some cases, oxidation can also be embraced as a productive strategy by which valuable new transformations can be realized. This proposal targets both of these issues. For cross-coupling reactions that generate new C-C and C-N bonds, the inclusion of anti-oxidant additives will be explored with the anticipated benefit of expanding the applicability of these transformations to those that may previously have been hindered such as couplings with sensitive sulfur, oxygen, or boron-containing functional groups. Towards harnessing oxidation, the transient oxidation of amines to hydroxylamines will be exploited to develop new stoichiometric and catalytic C-N bond forming reactions via hydroamination pathways, providing a new way to access saturated nitrogen-containing heterocycles. Applications of these methods to access novel molecular space for the discovery of new drugs will be carried out in close collaboration with industrial partners who have previously struggled with these challenges in redox chemistry.