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Grant: Discovery Grants Program - Individual

University of Lethbridge

$25,000.00

New Catalytic Methodologies for the Synthesis of Organofluorine Compounds

FY 2023-24

Summary
Fluorine incorporation into organic compounds poses minimal steric constraints, but its strong electron-withdrawing ability can cause a modulation of the pKa of neighbouring functional groups or the energy of frontier orbitals. Fluorine can also strengthen or participate in key intra- and intermolecular electrostatic interactions. As a result of the effects caused by fluorine incorporation, it has become key to the design of drugs, agrochemical agents, and advanced materials among other areas. This is remarkable as fluorine is virtually absent from naturally occurring organic compounds, and there is now a growing need for robust methods to access and build complexity into organofluorine compounds. Furthermore, sustainable syntheses are highly desirable and may come from improved reaction conditions minimizing chemical wastes, and from novel disconnections enabling short syntheses. Transition-metal catalysis may be a key tool to engage organic compounds into new reactivity patterns, streamlining the synthesis of fluorinated molecules via reliable and step-efficient processes. Thus, the overarching goals of this research program will be (1) to manipulate C-H and C-C bonds to better access and derivatize organofluorine compounds; (2) to establish processes for preparing strained or fused, fluorinated cyclic compounds, and investigate their novel applications towards new fluorinated motifs; and (3) to explore the bioisosterism of new fluorinated motifs and their potential as molecular probes. Over the next five years, under this Discovery Grant, graduate and undergraduate students involved in my research activities will develop new synthetic routes to fluorinated molecules by exploiting C-H and C-C bonds as handles for functionalization, and will expand on the reactivity, installation, and applications of strained fluorinated carbocycles, particularly bicyclo[1.1.1]pentanyl derivatives and gem-difluorocyclopropanes. The overall research program will result in major advances that will influence how we construct and manipulate organofluorine compound, benefiting academia, the Canadian industry (e.g. pharmaceutical, agrochemical), and efforts in R&D at large.
Program
Discovery Grants Program - Individual
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
RGPIN-2022-04290
Name nom
Hamel, Jean-Denys
Department département
Chemistry and Biochemistry
Organization id
12
Institution établissement
University of Lethbridge
Province en
Alberta
Province fr
Alberta
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2022
Award amount
25000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
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
3704
Research subject group en
Organic chemistry
Research subject group fr
Synthetic methodology
Research subject en
Chimie organique
Research subject fr
Méthodologie en synthèse
Application title
New Catalytic Methodologies for the Synthesis of Organofluorine Compounds
Keyword
Alkyl Fluorides; Catalysis; C-C Bond Functionalization; C-H Bond Functionalization; Enantioselective Synthesis; Fluorination; Green Chemistry; Organic Synthesis; Organofluorine Chemistry; Vinyl fluorides
Application summary
Fluorine incorporation into organic compounds poses minimal steric constraints, but its strong electron-withdrawing ability can cause a modulation of the pKa of neighbouring functional groups or the energy of frontier orbitals. Fluorine can also strengthen or participate in key intra- and intermolecular electrostatic interactions. As a result of the effects caused by fluorine incorporation, it has become key to the design of drugs, agrochemical agents, and advanced materials among other areas. This is remarkable as fluorine is virtually absent from naturally occurring organic compounds, and there is now a growing need for robust methods to access and build complexity into organofluorine compounds. Furthermore, sustainable syntheses are highly desirable and may come from improved reaction conditions minimizing chemical wastes, and from novel disconnections enabling short syntheses. Transition-metal catalysis may be a key tool to engage organic compounds into new reactivity patterns, streamlining the synthesis of fluorinated molecules via reliable and step-efficient processes. Thus, the overarching goals of this research program will be (1) to manipulate C-H and C-C bonds to better access and derivatize organofluorine compounds; (2) to establish processes for preparing strained or fused, fluorinated cyclic compounds, and investigate their novel applications towards new fluorinated motifs; and (3) to explore the bioisosterism of new fluorinated motifs and their potential as molecular probes. Over the next five years, under this Discovery Grant, graduate and undergraduate students involved in my research activities will develop new synthetic routes to fluorinated molecules by exploiting C-H and C-C bonds as handles for functionalization, and will expand on the reactivity, installation, and applications of strained fluorinated carbocycles, particularly bicyclo[1.1.1]pentanyl derivatives and gem-difluorocyclopropanes. The overall research program will result in major advances that will influence how we construct and manipulate organofluorine compound, benefiting academia, the Canadian industry (e.g. pharmaceutical, agrochemical), and efforts in R&D at large.