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Grant: Discovery Grants Program - Individual

Université du Québec à Montréal

$36,000.00

Total synthesis of alkaloid natural products and development of new synthetic tools

EF 2021-22

Résumé
The discovery of new strategies for the synthesis of complex natural products represents a continuing challenge and is crucial for finding new important applications in medicine and materials science. Most of the compounds demonstrating biological properties possess a heterocyclic or a polycyclic skeleton such as alkaloids and related natural products. Unfortunately, the natural amount of these products is generally low and would require damaging an ecosystem to provide treatments. This fundamental research program aims to discover new synthetic tools to produce the main core of these structures quickly, their analogs and ultimately the targeted natural products. In this context, the research program presented in this proposal will be divided into two different and complementary parts dedicated to the elaboration of novel environmentally-friendly methodologies enabling the rapid formation of heterocyclic or cyclic motifs as well as applications of similar processes recently developed by the laboratory for the total synthesis of natural products. This proposal highlights new tools for the rapid and environmentally conscious synthesis of polyfunctionalized scaffolds involving mild, user-friendly conditions to produce the main core of natural products. New synthetic tools in heterocyclic chemistry to produce pyridine, 2-pyridone, furan and pyrroles are presented as well as an oxidative variant of the Conia-ene transformation. In addition, we propose the stereoselective total synthesis of seven alkaloids or related products such as deoxyaspidodispermine, valiolamine/voglibose, homolycorine, huperzimine, cepharatine, (dihydro)-lycoricidine and hispidospermidin. Some of these syntheses are based on a functional protecting group or a functional chiral auxiliary, which are not only a functionality moderator or a chirality inductor but also final moieties of the target. Students involved in total synthesis projects will receive a good formation; they will be trained in the concepts and methods of modern synthetic organic chemistry. Personnel with expertise in this field are very much in demand in the public and in private sectors, especially in the pharmaceutical industry.
Programme
Discovery Grants Program - Individual
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
RGPIN-2021-03305
Name nom
Canesi, Sylvain
Department département
Chemistry
Organization id
57
Institution établissement
Université du Québec à Montréal
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2021
Competition year année de concours
2021
Award amount
36000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1504
Committee name en
Chemistry
Committee name fr
Chimie
Area of application code
1202
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Physical sciences
Area of application fr
Sciences physiques
Research subject code
3704
Research subject group en
Organic chemistry
Research subject group fr
Chimie organique
Research subject en
Synthetic methodology
Research subject fr
Méthodologie en synthèse
Installment
inst:1
Partie
1
Nb partie
5
Application title
Total synthesis of alkaloid natural products and development of new synthetic tools
Keyword
NSERC
Application summary
The discovery of new strategies for the synthesis of complex natural products represents a continuing challenge and is crucial for finding new important applications in medicine and materials science. Most of the compounds demonstrating biological properties possess a heterocyclic or a polycyclic skeleton such as alkaloids and related natural products. Unfortunately, the natural amount of these products is generally low and would require damaging an ecosystem to provide treatments. This fundamental research program aims to discover new synthetic tools to produce the main core of these structures quickly, their analogs and ultimately the targeted natural products. In this context, the research program presented in this proposal will be divided into two different and complementary parts dedicated to the elaboration of novel environmentally-friendly methodologies enabling the rapid formation of heterocyclic or cyclic motifs as well as applications of similar processes recently developed by the laboratory for the total synthesis of natural products. This proposal highlights new tools for the rapid and environmentally conscious synthesis of polyfunctionalized scaffolds involving mild, user-friendly conditions to produce the main core of natural products. New synthetic tools in heterocyclic chemistry to produce pyridine, 2-pyridone, furan and pyrroles are presented as well as an oxidative variant of the Conia-ene transformation. In addition, we propose the stereoselective total synthesis of seven alkaloids or related products such as deoxyaspidodispermine, valiolamine/voglibose, homolycorine, huperzimine, cepharatine, (dihydro)-lycoricidine and hispidospermidin. Some of these syntheses are based on a functional protecting group or a functional chiral auxiliary, which are not only a functionality moderator or a chirality inductor but also final moieties of the target. Students involved in total synthesis projects will receive a good formation; they will be trained in the concepts and methods of modern synthetic organic chemistry. Personnel with expertise in this field are very much in demand in the public and in private sectors, especially in the pharmaceutical industry.