{"id":18644,"date":"2024-04-11T10:11:19","date_gmt":"2024-04-11T14:11:19","guid":{"rendered":"https:\/\/www.uqar.ca\/personnes\/sebastien-cardinal\/"},"modified":"2026-07-08T00:15:46","modified_gmt":"2026-07-08T04:15:46","slug":"cardinal-sebastien","status":"publish","type":"personnes","link":"https:\/\/www.uqar.ca\/en\/professeurs\/cardinal-sebastien\/","title":{"rendered":"S\u00e9bastien Cardinal"},"content":{"rendered":"\n<section class=\"wp-block-stereo-section-bloc section-block-small -section-block-padding-sm\" data-stereo-anchor-name=\"\"><div class=\"wp-block-stereo-section__container\"><div class=\"wp-block-stereo-section__col is-layout-flow wp-block-stereo-section-bloc-is-layout-flow\">\n<div class=\"wp-block-create-block-accordion-block\"><div class=\"c-tabs\" data-module=\"Tabs\"><div class=\"c-tabs-nav__wrap\" role=\"tablist\"><div class=\"c-tabs-nav-mobile\"><button data-tabs=\"button\" tabindex=\"0\" data-tabs-dir=\"<\" class=\"c-tabs-nav-mobile__button\" role=\"tab\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-left\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg#arrow-left\"><\/use><\/svg><\/button><button data-tabs=\"button\" tabindex=\"0\" data-tabs-dir=\"&gt;\" class=\"c-tabs-nav-mobile__button\" role=\"tab\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-right\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg#arrow-right\"><\/use><\/svg><\/button><\/div><div class=\"c-tabs-nav\" data-tabs=\"nav\"><button class=\"c-tabs-nav__item\" data-tabs=\"trigger\" role=\"tab\"><span class=\"c-tab\">Pages Web<\/span><\/button><button class=\"c-tabs-nav__item\" data-tabs=\"trigger\" role=\"tab\"><span class=\"c-tab\">Recherches et expertises<\/span><\/button><button class=\"c-tabs-nav__item\" data-tabs=\"trigger\" role=\"tab\"><span class=\"c-tab\">Publications et communications<\/span><\/button><button class=\"c-tabs-nav__item\" data-tabs=\"trigger\" role=\"tab\"><span class=\"c-tab\">Cours enseign\u00e9s<\/span><\/button><\/div><\/div><div class=\"c-tabs-content__wrap\">\n<div class=\"c-tab-content__item\" data-tabs=\"content\"><div class=\"c-tab-content\">\n<p><a href=\"http:\/\/www.labocardinal.ca\" target=\"_blank\" rel=\"noreferrer noopener\">Laboratoire Cardinal<\/a> (page personnelle)<\/p>\n\n\n\n<p><a href=\"https:\/\/www.uqar.ca\/recherche\/la-recherche-a-l-uqar\/unites-de-recherche\/groupe-de-recherche-sur-les-environnements-nordiques-boreas\/presentation-objectifs-et-mission-boreas\" target=\"_blank\" rel=\"noreferrer noopener\">Groupe de recherche sur les environnements nordiques BOR\u00c9AS<\/a><\/p>\n\n\n\n<p><a href=\"https:\/\/www.uqar.ca\/recherche\/unites-de-recherche\/collectif-de-recherche-appliquee-aux-bioprocedes-et-a-la-chimie-de-lenvironnement-crabe\/\" data-type=\"link\" data-id=\"https:\/\/www.uqar.ca\/recherche\/unites-de-recherche\/collectif-de-recherche-appliquee-aux-bioprocedes-et-a-la-chimie-de-lenvironnement-crabe\/\" target=\"_blank\" rel=\"noreferrer noopener\">Regroupement CRABE<\/a><\/p>\n<\/div><\/div>\n\n\n\n<div class=\"c-tab-content__item\" data-tabs=\"content\"><div class=\"c-tab-content\">\n<div class=\"wp-block-create-block-accordion-block\"><div class=\"c-accordion\" data-module=\"Accordion\" data-accordion-toggle=\"true\" data-accordion-scroll=\"true\" data-accordion-preopen=\"-1\">\n<div class=\"c-accordion__section\" data-accordion=\"wrap\"><button type=\"button\" aria-label=\"Ouvrir  Formation\" class=\"c-accordion__header\" data-accordion=\"trigger\"><span class=\"c-accordion__header__title\" id=\"formation\"><span class=\"c-accordion__button\"> Formation<span class=\"c-accordion__header__icon\"><span class=\"o-button__icon\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-down\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg?v=4ffa4cbaabe44c792c?v=4ffa4cbaabe44c792c#arrow-down\"><\/use><\/svg><\/span><\/span><\/span><\/span><\/button><div class=\"c-accordion__content\" role=\"region\" data-accordion=\"content\"><div class=\"c-accordion__inner\">\n<ul class=\"wp-block-list\">\n<li>Postdoctoral Fellow, Princeton University (2017-2018)<\/li>\n\n\n\n<li>Ph.D. chimie, Universit\u00e9 Laval (2016)<\/li>\n\n\n\n<li>B.Sc. chimie, Universit\u00e9 Laval (2009)<\/li>\n<\/ul>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"c-accordion__section\" data-accordion=\"wrap\"><button type=\"button\" aria-label=\"Ouvrir  Projets de recherche en cours et subventions\" class=\"c-accordion__header\" data-accordion=\"trigger\"><span class=\"c-accordion__header__title\" id=\"projets-de-recherche-en-cours-et-subventions\"><span class=\"c-accordion__button\"> Projets de recherche en cours et subventions<span class=\"c-accordion__header__icon\"><span class=\"o-button__icon\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-down\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg?v=4ffa4cbaabe44c792c?v=4ffa4cbaabe44c792c#arrow-down\"><\/use><\/svg><\/span><\/span><\/span><\/span><\/button><div class=\"c-accordion__content\" role=\"region\" data-accordion=\"content\"><div class=\"c-accordion__inner\">\n<h4 class=\"wp-block-heading\"><strong>Axe de recherche 1<\/strong><\/h4>\n\n\n\n<p><strong>La catalyse photor\u00e9dox comme voie d\u2019acc\u00e8s \u00e0 des librairies de compos\u00e9s d\u2019int\u00e9r\u00eat biologique.<\/strong><\/p>\n\n\n\n<p>La catalyse photor\u00e9dox s\u2019est impos\u00e9e dans la derni\u00e8re d\u00e9cennie comme un outil r\u00e9volutionnaire pour la synth\u00e8se organique, tant dans la recherche acad\u00e9mique que dans l\u2019industrie pharmaceutique. &nbsp;Ce type de catalyse, dans lequel le catalyseur est activ\u00e9 par l\u2019action de la lumi\u00e8re visible, permet d\u2019acc\u00e9der, dans des conditions r\u00e9actionnelles douces et s\u00e9curitaires, \u00e0 des voies m\u00e9canistiques n\u00e9cessitant g\u00e9n\u00e9ralement de la radiation UV ou d\u2019autres voies d\u2019activation hautement \u00e9nerg\u00e9tiques. Notamment, la catalyse photor\u00e9dox permet, dans un contexte contr\u00f4l\u00e9, le d\u00e9veloppement de r\u00e9action n\u00e9cessitant la g\u00e9n\u00e9ration de radicaux libres ou ayant recours \u00e0 un transfert d\u2019\u00e9nergie de type triplet-triplet. Un aspect d\u00e9terminant \u00e0 l\u2019ascension fulgurante de la catalyse photor\u00e9dox en synth\u00e8se organique est le fait qu\u2019elle puisse \u00eatre utilis\u00e9e en tandem avec un syst\u00e8me catalytique classique bas\u00e9 sur un m\u00e9tal de transition. Ce type de catalyse, qualifi\u00e9 de m\u00e9tallaphotor\u00e9dox, a, entre autres choses, r\u00e9volutionn\u00e9 les r\u00e9actions de couplages crois\u00e9s classiques en permettant de nouvelles combinaisons in\u00e9dites de partenaires. En somme, en d\u00e9bloquant des voies m\u00e9canistiques in\u00e9dites, la catalyse photor\u00e9dox\/m\u00e9tallaphotor\u00e9dox permet d\u2019envisager de nouvelles d\u00e9connections chimiques et l\u2019activation de groupements fonctionnels selon des voies in\u00e9dites.<\/p>\n\n\n\n<p>Dans le cadre de cet axe de recherche, mon \u00e9quipe et moi-m\u00eame visons \u00e0 tirer profit de la polyvalence et de la puissance de ce type d\u2019activation afin de d\u00e9velopper de nouvelles strat\u00e9gies permettant d\u2019acc\u00e9der plus facilement \u00e0 des librairies de compos\u00e9s difficiles d\u2019acc\u00e8s, mais ayant un int\u00e9r\u00eat biologique. L\u2019atteinte de cet objectif global peut s\u2019effectuer de deux mani\u00e8res, soit par le d\u00e9veloppement de r\u00e9actions in\u00e9dites ou par l\u2019application (l\u2019extension) de r\u00e9actions existantes \u00e0 d\u2019autres motifs mol\u00e9culaires plus complexes. En parall\u00e8le, nous visons mettre \u00e0 profit les librairies pr\u00e9par\u00e9es via l\u2019\u00e9tablissement de collaborations acad\u00e9miques ou industrielles.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Axe de recherche 2<\/strong><\/h4>\n\n\n\n<p><strong>Synth\u00e8se totale et \u00e9tude de l\u2019activit\u00e9 biologique de produits naturels locaux et d\u2019analogues<\/strong><\/p>\n\n\n\n<p>Bien que la chimie des produits naturels demeure un champ de recherche d\u2019int\u00e9r\u00eat mondial, une grande part des travaux dans cette discipline demeurent concentr\u00e9s sur l\u2019\u00e9tude d\u2019un nombre restreint d\u2019\u00e9cosyst\u00e8mes et certaines r\u00e9gions du globe demeurent peu investigu\u00e9es. Les \u00e9cosyst\u00e8mes qu\u00e9b\u00e9cois (surtout subarctiques et arctiques) constituent des exemples notables de r\u00e9servoirs sous-exploit\u00e9s en science des produits naturels. \u00c9tant soumise \u00e0 des stress environnementaux de natures multiples, la biodiversit\u00e9 occupant ces r\u00e9gions pr\u00e9sente un int\u00e9r\u00eat d\u2019autant plus grand vu son potentiel \u00e0 produire des m\u00e9tabolites secondaires couvrant un large spectre d\u2019activit\u00e9s biologiques. Heureusement, de plus en plus de groupes de recherche s\u2019int\u00e9ressent \u00e0 explorer la composition mol\u00e9culaire des \u00e9cosyst\u00e8mes composant notre territoire qu\u00e9b\u00e9cois. Bien que ces efforts de recherche aient men\u00e9 \u00e0 l\u2019identification de produits naturels d\u2019int\u00e9r\u00eat, l\u2019\u00e9tude de l\u2019activit\u00e9 biologique de ces mol\u00e9cules demeure la plupart du temps limit\u00e9 par leur faible abondance dans leur biomasse d\u2019origine. En r\u00e9ponse \u00e0 cette probl\u00e9matique, cet axe de recherche vise \u00e0 acc\u00e9l\u00e9rer l\u2019avancement des connaissances et la mise en valeur de la diversit\u00e9 mol\u00e9culaire des \u00e9cosyst\u00e8mes qu\u00e9b\u00e9cois via le d\u00e9veloppement de voies de synth\u00e8se chimique.<\/p>\n\n\n\n<p>En plus, de faire la synth\u00e8se totale des mol\u00e9cules cibl\u00e9es, nous travaillons, dans le cadre de cet axe de recherche, \u00e0 d\u00e9velopper un r\u00e9seau de collaboratrices et de collaborateurs, de mani\u00e8re \u00e0 nous impliquer directement dans l\u2019\u00e9tude des propri\u00e9t\u00e9s biologiques des produits naturels synth\u00e9tis\u00e9s. En ce sens, la synth\u00e8se d\u2019analogues est \u00e9galement fr\u00e9quemment r\u00e9alis\u00e9e dans le but de pouvoir mener des \u00e9tudes de relation structure-activit\u00e9.<\/p>\n\n\n\n<p>Finalement, ce programme de recherche, bien qu\u2019orient\u00e9 sur l\u2019obtention de mol\u00e9cules pr\u00e9cises, peut \u00e9galement s\u2019av\u00e9rer un contexte favorable au d\u00e9veloppement de nouvelles r\u00e9actions (ou de nouveaux syst\u00e8mes r\u00e9actionnels) permettant d\u2019atteindre les structures cibl\u00e9es plus efficacement.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Axe de recherche 3<\/strong><\/h4>\n\n\n\n<p><strong>Valorisation de la biomasse locale pour des applications \u00e0 haute valeur ajout\u00e9e et \u00e0 impact environnemental positif<\/strong><\/p>\n\n\n\n<p>Les r\u00e9gions de l\u2019Est du Qu\u00e9bec (Bas-St-Laurent, Gasp\u00e9sie, C\u00f4te-Nord) ont une industrie primaire importante. Bien que les produits g\u00e9n\u00e9r\u00e9s par celle-ci soient essentiels \u00e0 notre \u00e9conomie, la valeur de ceux-ci est g\u00e9n\u00e9ralement faible. \u00c9galement, ces industries g\u00e9n\u00e8rent des quantit\u00e9s importantes de d\u00e9chets (ou coproduits) dont la gestion peut \u00eatre probl\u00e9matique. Consid\u00e9rant ces deux r\u00e9alit\u00e9s, nous cherchons, dans le cadre de cet axe de recherche, \u00e0 proposer des solutions permettant de g\u00e9n\u00e9rer plus de valeur pour ces industries selon deux approches. D\u2019une part, nous travaillons \u00e0 d\u00e9velopper des applications \u00e0 plus haute valeur ajout\u00e9e pour certaines biomasses. D\u2019autre part, nous cherchons \u00e0 transformer certains coproduits en produits d\u2019int\u00e9r\u00eat commercial de plus grande valeur. Dans les deux cas, les applications vis\u00e9es s\u2019inscrivent \u00e9galement dans une perspective de d\u00e9veloppement durable, soit d\u2019offrir des alternatives biosourc\u00e9es \u00e0 des produits dommageables pour l\u2019environnement.<\/p>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Financement actuel<\/strong><\/h4>\n\n\n\n<p>CRSNG subvention \u00e0 la d\u00e9couverte (2024-2029); FRQNT projet de recherche en \u00e9quipe (2021-2025); R\u00e9seau qu\u00e9b\u00e9cois de recherche sur le m\u00e9dicament (RQRM), INAF Projet-Pilote.<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"c-accordion__section\" data-accordion=\"wrap\"><button type=\"button\" aria-label=\"Ouvrir  Supervision d'\u00e9tudiants de cycles sup\u00e9rieurs\" class=\"c-accordion__header\" data-accordion=\"trigger\"><span class=\"c-accordion__header__title\" id=\"supervision-detudiants-de-cycles-superieurs\"><span class=\"c-accordion__button\"> Supervision d&#8217;\u00e9tudiants de cycles sup\u00e9rieurs<span class=\"c-accordion__header__icon\"><span class=\"o-button__icon\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-down\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg?v=4ffa4cbaabe44c792c?v=4ffa4cbaabe44c792c#arrow-down\"><\/use><\/svg><\/span><\/span><\/span><\/span><\/button><div class=\"c-accordion__content\" role=\"region\" data-accordion=\"content\"><div class=\"c-accordion__inner\">\n<p><strong>\u00c9tudiantes et \u00e9tudiants \u00e0 la ma\u00eetrise en chimie de l&#8217;environnement et des bioproc\u00e9d\u00e9s <\/strong><\/p>\n\n\n\n<p>Fr\u00e9d\u00e9ric Potvin [2024-pr\u00e9sent]<\/p>\n\n\n\n<p class=\"has--color has-text-color\"><strong>\u00c9tudiantes et \u00e9tudiants \u00e0 la ma\u00eetrise sur mesure<br><\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Maxime Potvin [2023-pr\u00e9sent]<\/li>\n\n\n\n<li>Tommy Fraser [2019-2022]<\/li>\n\n\n\n<li>Amy McMackin [2020-2022]<\/li>\n<\/ul>\n\n\n\n<p><strong><strong>\u00c9tudiantes et \u00e9tudiants au doctorat<\/strong> sur mesure<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>C\u00e9line Dedieu [2025-pr\u00e9sent]<\/li>\n<\/ul>\n\n\n\n<p class=\"has--color has-text-color\"><strong><strong>\u00c9tudiantes et \u00e9tudiants au doctorat en oc\u00e9anographie<\/strong><\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Sarah Kefil [2022-pr\u00e9sent]<\/li>\n\n\n\n<li>\u00c9lise Heinen [2023-pr\u00e9sent]<\/li>\n<\/ul>\n\n\n\n<p>N\u2019h\u00e9sitez pas \u00e0 me contacter pour conna\u00eetre les opportunit\u00e9s en cours offertes dans le laboratoire (formation en chimie requise)!<\/p>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"c-accordion__section\" data-accordion=\"wrap\"><button type=\"button\" aria-label=\"Ouvrir  Exp\u00e9rience professionnelle\" class=\"c-accordion__header\" data-accordion=\"trigger\"><span class=\"c-accordion__header__title\" id=\"experience-professionnelle\"><span class=\"c-accordion__button\"> Exp\u00e9rience professionnelle<span class=\"c-accordion__header__icon\"><span class=\"o-button__icon\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-down\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg?v=4ffa4cbaabe44c792c?v=4ffa4cbaabe44c792c#arrow-down\"><\/use><\/svg><\/span><\/span><\/span><\/span><\/button><div class=\"c-accordion__content\" role=\"region\" data-accordion=\"content\"><div class=\"c-accordion__inner\">\n<ul class=\"wp-block-list\">\n<li>Professeur associ\u00e9, D\u00e9partement de chimie, Universit\u00e9 Laval (2024-)<\/li>\n\n\n\n<li>Charg\u00e9 de cours, D\u00e9partement de chimie de l\u2019Universit\u00e9 Laval (2012-2014)<\/li>\n<\/ul>\n<\/div><\/div><\/div>\n<\/div><\/div>\n<\/div><\/div>\n\n\n\n<div class=\"c-tab-content__item\" data-tabs=\"content\"><div class=\"c-tab-content\">\n<div class=\"wp-block-create-block-accordion-block\"><div class=\"c-accordion\" data-module=\"Accordion\" data-accordion-toggle=\"true\" data-accordion-scroll=\"true\" data-accordion-preopen=\"-1\">\n<div class=\"c-accordion__section\" data-accordion=\"wrap\"><button type=\"button\" aria-label=\"Ouvrir  Publications\" class=\"c-accordion__header\" data-accordion=\"trigger\"><span class=\"c-accordion__header__title\" id=\"publications\"><span class=\"c-accordion__button\"> Publications<span class=\"c-accordion__header__icon\"><span class=\"o-button__icon\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-down\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg?v=4ffa4cbaabe44c792c?v=4ffa4cbaabe44c792c#arrow-down\"><\/use><\/svg><\/span><\/span><\/span><\/span><\/button><div class=\"c-accordion__content\" role=\"region\" data-accordion=\"content\"><div class=\"c-accordion__inner\">\n<ul class=\"wp-block-list\">\n<li>McMackin, A., Cardinal, S. <em>Carbohydrate-Based Alternatives to Traditional Synthetic Plastic Microbeads: a critical review.<\/em> RSC Sustainability, <strong>2025<\/strong>, <em>3 (4),<\/em> 1629. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/su\/d4su00364k#!divAbstract\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>Fraser T., Harbour, Z.,Voyer, N., Cardinal S. <em>Chemo- and regioselective demethylation of 2-bromo-\u03b1-resorcylic acid derivatives using alkylthiolate salts<\/em>. Synlett. <strong>2025<\/strong>, <em>36 (5)<\/em>, <em>512.<\/em> [<a href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/a-2370-7112\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>Amamou O., Denis J.-P., Heinen E., Boubaker T., Cardinal S. <em>Revisiting the Determination of the Degree of Deacetylation Using Potentiometric Titration: A New Equation for Modified Chitosan<\/em>. Molecules, <strong>2024<\/strong>, <em>29(13)<\/em>, 2962. [<a href=\"https:\/\/www.mdpi.com\/1420-3049\/29\/13\/2962\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>McMackin A., Banville V., Cardinal S. <em>Biosourced Spherical Microbeads form Brewer&#8217;s Spent Grain for Sustainable Personal Hygiene Products <\/em>Journal of Polymer Science, <strong>2024<\/strong>, <em>62<\/em>, 2270-2287. [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/pola.31178\">Page couverture du journal<\/a>] [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/pol.20230613\">Acc\u00e8s \u00e0 l\u2019article]<\/a><\/li>\n\n\n\n<li>Amamou O., Denis J.-P., Heinen E., Boubaker T., Cardinal S. <em>A new and rapid HPLC method to determine the degree of deacetylation of glutaraldehyde-cross-linked chitosan<\/em>. Molecules, <strong>2023<\/strong>, <em>28(21)<\/em>, 7294. [<a href=\"https:\/\/www.mdpi.com\/1420-3049\/28\/21\/7294#:~:text=Herein%2C%20we%20report%20a%20new,glutaraldehyde%20after%20the%20reticulation%20reaction.\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>B\u00e9rub\u00e9 C., Guay L.-D., Fraser T., Lapointe V., Cardinal S., Biron E. <em>Convenient route to Fmoc- homotyrosine via metallaphotoredox catalysis and its use in the total synthesis of anabaenopeptin cyclic peptides.<\/em> Organic &amp; Biomolecular Chemistry, <strong>2023<\/strong>, <em>(21)<\/em>, 9011-9020. [<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2023\/ob\/d3ob01608k\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>Bouchard C, Grenier A, Cardinal S, B\u00e9langer S, Voyer N, Pouliot R. <em>Antipsoriatic Potential of Quebecol and Its Derivatives<\/em>, Pharmaceutics, <strong>2022<\/strong>, <em>14(6)<\/em>, 1129. [<a href=\"https:\/\/www.mdpi.com\/1999-4923\/14\/6\/1129\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>Cardinal, S.; Ben Lagha, A.&nbsp;; Azelmat, J.&nbsp;; Grenier, D. <em>Quebecol shows potential to alleviate periodontal tissue damage and promote bone formation in in vitro models, <\/em>ACS Omega, <strong>2021<\/strong>, <em>6(42), <\/em>27791-171. [<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acsomega.1c03312\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>Paquet-C\u00f4t\u00e9, P.-A.; Fillion, M.; Provencher, M.-\u00c8.; Otis, F.; Dionne, J.; Cardinal, S.; Collignon, B.; B\u00fcrck, J.; Lag\u00fce, P.; Ulrich, A.S.; Auger, M.; Voyer, N. <em>Crown ether modified peptide interactions with model membranes, <\/em>Supramolecular Chemistry, <strong>2019<\/strong>, <em>31, <\/em>159-171. [<a href=\"https:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/10610278.2019.1574349\">Acc\u00e8s \u00e0 l\u2019article<\/a>]<\/li>\n\n\n\n<li>Bacauanu, V.*; Cardinal, S.*; Yamauchi, M.*; Kondo, M.; Fern\u00e1ndez, D. F.; Remy, R.; MacMillan, D. W. C. <em>Metallaphotoredox Difluoromethylation of Aryl Bromides<\/em>,Angewante Chemie, Internationnal Edition,<strong>2018<\/strong>, <em>57, 12543-12548.<\/em> [<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201807629\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>Cardinal, S.; Paquet-C\u00f4t\u00e9, P.-A.; Azelmat, J.; Bouchard, C.; Grenier, D.; Voyer, N. <em>Synthesis and anti-inflammatory activity of isoquebecol<\/em>, Bioorganic and Medicinal Chemistry<em>,<\/em> <strong>2017<\/strong>, <em>25<\/em>, 2043-2056. [<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0968089616309403\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>B\u00e9rub\u00e9, C., Barbeau X., Cardinal, S., Boudreault, P.L., Bouchard, C., Delcey, N., Lag\u00fce P., Voyer, N. <em>Interfacial supramolecular biomimetic epoxidation catalysed by cyclic dipeptides<\/em>, Supramolecular Chemistry, <strong>2017<\/strong><em>, 29<\/em>, 330-349. [<a href=\"https:\/\/www.tandfonline.com\/doi\/abs\/10.1080\/10610278.2016.1236197\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. <em>Preparation of 2,3,3-triarylacrylic acid esters using Suzuki-Miyaura coupling reactions, <\/em>Synthesis, <strong>2016<\/strong>, <em>48<\/em>, 1202-1216. [<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0035-1560419\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>Cardinal, S., Azelmat, J., Grenier, D., Voyer, N. <em>Anti-inflammatory activity of quebecol and derivatives, <\/em>Bioorganic and Medicinal Chemistry Letters,<strong> 2016<\/strong>, <em>26<\/em>, 440-444. [<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0960894X15303048?via%3Dihub\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>B\u00e9rub\u00e9, C., Cardinal, S., Boudreault, P.L., Barbeau, X., Delcey, N., Gigu\u00e8re, M., Gleeton, D., Voyer, N. <em>Novel chiral N,N\u2019-dimethyl-1,4-piperazines with metal binding abilities, <\/em>Tetrahedron, <strong>2015<\/strong>, <em>71<\/em>, 8077-8084. [<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402015300053\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. <em>Total synthesis of quebecol<\/em>, Tetrahedron Letters, <strong>2013<\/strong>, <em>54,<\/em> 5178-5180. [<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403913011878\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>Lorin, A., No\u00ebl, M., Provencher, M.-E., Turcotte, <strong>V., Cardinal, S.,<\/strong> Lag\u00fce, P., Voyer, N., Auger, M. <em>Determining the Mode of Action Involved in th Antimicrobial Activity of Synthetic Peptides : A Solid-State NMR and FTIR Study, <\/em>Biophysical Journal, <strong>2012<\/strong>, <em>103<\/em>,&nbsp; 1470-1479. [<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0006349512009848\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>Lorin, A., No\u00ebl, M., Provencher, M.-E., Turcotte, V., Masson, C., Cardinal, S., Lag\u00fce, P., Voyer, N., Auger, M. <em>Revisiting peptide amphiphilicity for membrane pore formation<\/em>, Biochemistry, <strong>2011<\/strong>, <em>50<\/em>, 9409-9420. [<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/bi201335t\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n\n\n\n<li>Boudreault, P.L., Cardinal, S., Voyer, N. <em>Suzuki coupling reaction of o-aminomethylboronic acids, <\/em>Synlett, <strong>2010<\/strong>, <em>16<\/em>, 2449-2452. [<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0030-1258554\">Acc\u00e8s \u00e0 l&#8217;article<\/a>]<\/li>\n<\/ul>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"c-accordion__section\" data-accordion=\"wrap\"><button type=\"button\" aria-label=\"Ouvrir  Communications\" class=\"c-accordion__header\" data-accordion=\"trigger\"><span class=\"c-accordion__header__title\" id=\"communications\"><span class=\"c-accordion__button\"> Communications<span class=\"c-accordion__header__icon\"><span class=\"o-button__icon\"><svg aria-hidden=\"true\" focusable=\"false\" class=\"o-ico -icon-arrow-down\"><use xlink:href=\"\/app\/themes\/baserock\/assets\/img\/sprite.svg?v=4ffa4cbaabe44c792c?v=4ffa4cbaabe44c792c#arrow-down\"><\/use><\/svg><\/span><\/span><\/span><\/span><\/button><div class=\"c-accordion__content\" role=\"region\" data-accordion=\"content\"><div class=\"c-accordion__inner\">\n<h4 class=\"wp-block-heading has--color has-text-color\"><strong>Conf\u00e9rences donn\u00e9es \u00e0 titre de pr\u00e9sentateur<\/strong>&nbsp;&nbsp;&nbsp;&nbsp;<\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Cardinal S., McMackin A, Banville V. (2025). From microbeads to new fibrous materials: aiming for the complete valorization of brewer\u2019s spent grain. Canadian Chemistry Conference and Exhibition (CSC) 2025, Ottawa, Canada<\/li>\n\n\n\n<li>Cardinal S., McMackin A, Banville V. (2023). Biodegradable Spherical Microbeads from Brewer\u2019s Spent Grain for Sustainable Personal Hygiene. Canadian Chemistry Conference and Exhibition (CSC) 2023, Vancouver, Canada<\/li>\n\n\n\n<li>Cardinal S.,McMackin A*, Banville V. (2023). Valorization of brewer\u2019s spent grain for the production of more sustainable materials. Green Food Tech 2023, Montr\u00e9al.<\/li>\n\n\n\n<li>Cardinal S., McMackin A*, Banville V. (2023). Valorization of brewer&#8217;s spent grain for the production of more sustainable materials. ACS Spring 2023, Indianapolis, \u00c9tats-Unis.<\/li>\n\n\n\n<li>Cardinal S. (2022). La biomasse locale comme source d\u2019inspiration et d\u2019opportunit\u00e9 en chimie organique. S\u00e9rie de s\u00e9minaires du Master chimie Pharmaceutique de l&#8217;Universit\u00e9 de Tlemcen, Tlemcen [Virtuel], Alg\u00e9rie<\/li>\n\n\n\n<li>Cardinal S., Fraser T. (2021). Synthesis of new dibenzofuran compounds isolated from a Canadian arctic lichen. Pacifichem 2021, Honolulu [Virtuel], \u00c9tats-Unis. d&#8217;Am\u00e9rique.<\/li>\n\n\n\n<li>Cardinal S. (2021). La biomasse locale : source de d\u00e9couvertes et d\u2019opportunit\u00e9s en chimie organique. Conf\u00e9rences de l&#8217;INAF, Qu\u00e9bec, Canada<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2015) <em>Stereoselective preparation of 2,3,3-triarylacrylic acid esters using Suzuki-Miyaura coupling reactions.<\/em> Pacifichem 2015, Honolulu, \u00c9tats-Unis.<\/li>\n\n\n\n<li>Cardinal, S., Azelmat, J., Grenier, D., Voyer, N. (2015) <em>New Approach Leading to Various 1,2,2-triarylethene Compounds : Application to the Total Synthesis of a Polyphenoclic Compound Found in Maple Syrup.<\/em> 26<sup>th<\/sup> Quebec-Ontario Mini-Symposium on Bioorganic and Organic Chemistry (QOMSBOC), Montr\u00e9al, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2015) <em>New Approach Leading to Various 1,2,2-triarylethene Compounds : Application to the Total Synthesis of a Polyphenoclic Compound Found in Maple Syrup.<\/em> Congr\u00e8s canadien de chimie et exposition de la Soci\u00e9t\u00e9 canadienne de chimie (SCC), Ottawa, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2014) <em>New approaches leading to 1,2,2-triarylethane and 1,2,2-triarylethene moieties: Application to the total synthesis of a polyphenoclic compound found in maple syrup. <\/em>248th ACS National Meeting, San Francisco, \u00c9tats-Unis.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2013) <em>Synthesis of a New Polyphenolic Compound found in Maple Syrup. <\/em>IUPAC World Chemistry Congress, Istanbul, Turquie.<\/li>\n\n\n\n<li>Cardinal, S., Boudreault, P.L., Voyer, N. (2012) <em>Progr\u00e8s vers la synth\u00e8se d\u2019allocolchicino\u00efdes. <\/em>80<sup>e<\/sup> congr\u00e8s de l\u2019Association francophone pour le savoir (ACFAS), Montr\u00e9al, Canada.<\/li>\n<\/ul>\n\n\n\n<h4 class=\"wp-block-heading has--color has-text-color\"><strong>Pr\u00e9sentations par affiche \u00e0 titre de pr\u00e9sentateur<\/strong><\/h4>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Cardinal, S., MacMillan, D.W.C. (2018) <em>Revisiting metallaphotoredox cross electrophile coupling for the construction of challenging C-C bonds. <\/em>255<sup>th<\/sup> American Chemical Society (ACS) National Meeting, Nouvelles-Orl\u00e9ans, \u00c9tats-Unis.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2016) <em>Preparation of Various 2,3,3-triarylacrylic Acid Esters, a particular Class of 1,2,2-triarylethene Compounds, using Suzuki-Miyaura Coupling (SMC) Reactions<\/em>. 16<sup>e<\/sup> symposium annuel de PROTEO, Qu\u00e9bec, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2015) <em>Preparation of Various 2,3,3-triarylacrylic Acid Esters, a particular Class of 1,2,2-triarylethene Compounds, using Suzuki-Miyaura Coupling (SMC) Reactions<\/em>. 15<sup>e<\/sup> symposium annuel de PROTEO, Qu\u00e9bec, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2014) <em>Synthesis of a New Polyphenolic Compound found in Maple Syrup. <\/em>symposium annuel de PROTEO, Qu\u00e9bec, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2013) <em>Synthesis of a New Polyphenolic Compound found in Maple Syrup. <\/em>24<sup>th<\/sup> Quebec-Ontraio Mini-Symposium on Bioorganic and Organic Chemistry (QOMSBOC), Sherbrooke, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Voyer, N. (2013) <em>Synthesis of a New Polyphenolic Compound found in Maple Syrup. <\/em>96<sup>e<\/sup> congr\u00e8s canadien de chimie et exposition de la Soci\u00e9t\u00e9 canadienne de chimie (SCC), Qu\u00e9bec, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Boudreault, P.L., Voyer, N. (2013) <em>Towards a new enantioselective synthetic methodology of allocolchicino\u00efds. <\/em>13<sup>e<\/sup> symposium annuel de PROTEO, Laval, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Boudreault, P.L., Voyer, N. (2011) <em>Towards a new enantioselective synthetic methodology of allocolchicino\u00efds. <\/em>Pr\u00e9sentation par affiche au 94<sup>e<\/sup> congr\u00e8s canadien de chimie et exposition de la Soci\u00e9t\u00e9 canadienne de chimie (SCC), Montr\u00e9al, Canada.<\/li>\n\n\n\n<li>Cardinal, S., Boudreault, P.L., Voyer, N. (2010) <em>Towards a new enantioselective synthetic methodology of allocolchicino\u00efds. <\/em>Pr\u00e9sentation par affiche \u00e0 Pacifichem 2010, Honolulu, \u00c9tats-Unis.<\/li>\n<\/ul>\n<\/div><\/div><\/div>\n<\/div><\/div>\n<\/div><\/div>\n\n\n\n<div class=\"c-tab-content__item\" data-tabs=\"content\"><div class=\"c-tab-content\">\n    <p><strong>Premier cycle :<\/strong><\/p>\n    <ul>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB11109<\/a> Biomol\u00e9cules<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB16207<\/a> Outils de caract\u00e9risation mol\u00e9culaire<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB17309<\/a> Techniques g\u00e9n\u00e9rales de laboratoire II<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB19812<\/a> Stage en milieu de pratique I<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB21309<\/a> Produits naturels : transformations et analyses<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB29812<\/a> Stage en milieu de pratique II<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB31609<\/a> Proc\u00e9d\u00e9s d&#8217;extraction et de purification<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CHI10318<\/a> Chimie organique<\/li>\n            <\/ul>\n    <p><strong>Deuxi\u00e8me cycle :<\/strong><\/p>\n    <ul>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB74024<\/a> Synth\u00e8se organique avanc\u00e9e<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">CEB79124<\/a> Lectures dirig\u00e9es en chimie de l\u2019environnement et bioproc\u00e9d\u00e9s<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">FAU71417<\/a> S\u00e9minaire de recherche<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">GEO60319<\/a> Lectures dirig\u00e9es<\/li>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">ING74922<\/a> Lectures dirig\u00e9es<\/li>\n            <\/ul>\n    <p><strong>Troisi\u00e8me cycle :<\/strong><\/p>\n    <ul>\n                    <li><a target=\"_blank\" href=\"\" rel=\"noopener noreferrer\" class=\"no-barba\" aria-label=\"Ouvre dans une nouvelle fen\u00eatre\" tabindex=\"0\">6DIG990<\/a> Examen doctoral<\/li>\n            <\/ul>\n<\/div><\/div>\n<\/div><\/div><\/div>\n<\/div><\/div><\/section>\n","protected":false},"featured_media":47316,"template":"","departement_personnes":[261],"class_list":["post-18644","personnes","type-personnes","status-publish","has-post-thumbnail","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/personnes\/18644","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/personnes"}],"about":[{"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/types\/personnes"}],"version-history":[{"count":18,"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/personnes\/18644\/revisions"}],"predecessor-version":[{"id":73694,"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/personnes\/18644\/revisions\/73694"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/media\/47316"}],"wp:attachment":[{"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/media?parent=18644"}],"wp:term":[{"taxonomy":"departement_personnes","embeddable":true,"href":"https:\/\/www.uqar.ca\/en\/wp-json\/wp\/v2\/departement_personnes?post=18644"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}