dat@UBFCdat@UBFC search : keyword:"heterocyclic compounds"dat@UBFC websitehttps://search-data.ubfc.fr/custom/logo/icon/100.pnghttps://search-data.ubfc.fr/custom/logo/full/105h.pnghttps://search-data.ubfc.fr/search.php?s=keyword%3A%22heterocyclic+compounds%22&format=atom&lang=en2023-07-06T16:26:12Z4′-(N-(Propargyl)pyrrol-2-yl)-2,2′:6′,2′′-terpyridinehttps://search-data.ubfc.fr/FR-13002091000019-2023-07-06_4-N-Propargyl-pyrrol-2-yl-2-2-6-2-terpyridin.html#maj202307061826122023-07-06T16:26:12Z2023-07-06T16:26:12ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent Guyard
<p>A new terpyridine molecule, bearing a N-propargylated pyrrole, was prepared and characterized. Its synthesis was based on a Krohnke-type reaction between 2-acetylpyridine and N-propargylpyrrole-2-carboxaldehyde in a basic medium. An allene-containing terpyridine was also obtained as a by-product.</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2018 to 2019</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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AttributionNew spiropyrrolothiazole derivatives bearing an oxazolone moiety as potential antidiabetic agent: Design, synthesis, crystal structure, Hirshfeld surface analysis, ADME and molecular docking studieshttps://search-data.ubfc.fr/FR-18008901306731-2022-05-20-02_New-spiropyrrolothiazole-derivatives-bearing-an.html#maj202205201508222022-05-20T13:08:22Z2022-05-20T13:08:22ZKaïss AouadiMejdi SnoussiManel Ben HammoudaAnouar El HassaneMohedinne AskriAdel KadriAnna KruppKhaled HamdenMichael Knorrhttps://www.utinam.cnrs.fr/?Michael-KNORRLukas BriegerCarsten StrohmannSarra Boudriga
<p>In a sustained search for novel and effective antihyperglycemics, a new series of fifteen isomeric oxazolone-fused dispiropyrrolothiazoles resulting from one-pot three component reaction between L-4-thiazolidine carboxylic acid, arylidene-oxazolones and isatin (or acenaphthenequinone) has been ...</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3Acrystallography">crystallography</a>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22mathematical+%26+computational+biology%22">mathematical & computational biology</a>
...
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<div><strong>Collected date :</strong> from 2017 to 2020</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Manel+Ben+Hammouda%22">Manel Ben Hammouda</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Sarra+Boudriga%22">Sarra Boudriga</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Khaled+Hamden%22">Khaled Hamden</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Mohedinne+Askri%22">Mohedinne Askri</a>
...
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Attribution4′-(5-Methylfuran-2-yl)-2,2′:6′,2″-terpyridine: A New Ligand Obtained from a Biomass-Derived Aldehyde with Potential Application in Metal-Catalyzed Reactionshttps://search-data.ubfc.fr/FR-18008901306731-2021-10-01_4-5-Methylfuran-2-yl-2-2-6-2-terpyridine-A.html#maj202110010856442021-10-01T06:56:44Z2021-10-01T06:56:44ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent Guyard
<p>The new ligand 4′-(5-methylfuran-2-yl)-2,2′:6′,2″-terpyridine (1) was prepared in one step from 2-acetylpyridine and 5-methylfurfural. The latter is an aldehyde that can be readily obtained from biomass. The new terpyridine molecule was characterized by 1H and 13C-NMR spectroscopy as well as by ...</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2017 to 2018</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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</div>
Attribution4,4″-Dichloro-4′-(2-thienyl)-2,2′:6′,2″-terpyridinehttps://search-data.ubfc.fr/FR-18008901306731-2021-09-24-02_4-4-Dichloro-4-2-thienyl-2-2-6-2-terpyridin.html#maj202109241053562021-09-24T08:53:56Z2021-09-24T08:53:56ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-Jerome
<p>A new thiophene-substituted terpyridine derivative has been prepared and characterized. This ligand features a thiophene heterocycle (as an electrochemically polymerizable unit) as well as two chlorine atoms for further functionalization.</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
</div>
<div><strong>Collected date :</strong> from 2017 to 2018</div>
<div>
<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
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Attribution4′-(N-(Propan-1,2-dienyl)pyrrol-2-yl)-2,2′:6′,2″-terpyridinehttps://search-data.ubfc.fr/FR-18008901306731-2021-09-24_4-N-Propan-1-2-dienyl-pyrrol-2-yl-2-2-6-2-terpyridin.html#maj202109241053362021-09-24T08:53:36Z2021-09-24T08:53:36ZLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-Jerome
<p>A new pyrrole-substituted terpyridine derivative that possesses an allene moiety was obtained as an “unexpected” sole product during an attempt to alkylate the N-atom of pyrrole with propargyl bromide in order to obtain an alkyne-functionalized terpyridine. </p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
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<div><strong>Collected date :</strong> from 2018 to 2019</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
</div>
</div>
Attribution4′-(5-n-Propylthiophen-2-yl)-2,2′:6′,2″-terpyridine https://search-data.ubfc.fr/FR-18008901306731-2021-04-12-05_4-5-n-Propylthiophen-2-yl-2-2-6-2-terpyridine.html#maj202109101650172021-04-12T12:01:31Z2021-09-10T14:50:17ZJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-JeromeLaurent GuyardLaurent GuyardJérôme Hussonhttps://www.utinam.cnrs.fr/?Husson-Jerome
<p>A new thiophene-substituted terpyridine derivative has been prepared through the reaction between 5-n-propylthiophene-2-carboxaldehyde and 2-acetylpyridine. This terpyridine derivative bears an alkyl chain linked via a thiophene heterocycle. </p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+organic%22">chemistry, organic</a>
</div>
<div><strong>Collected date :</strong> 2020</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22J%C3%A9r%C3%B4me+Husson%22">Jérôme Husson</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
</div>
</div>
Attribution2-(2,2-Dibromoethenyl)thiophenehttps://search-data.ubfc.fr/FR-18008901306731-2016-08-23-04_2-2-2-Dibromo-ethen-yl-thio-phene.html#maj201608231157352016-08-23T09:57:35Z2016-08-23T09:57:35ZSébastien ClémentMichael Knorrhttps://www.utinam.cnrs.fr/?Michael-KNORRLaurent GuyardPrisca EckertCarsten Strohmann
<p>The title compound, C6H4Br2S, represents a versatile building block for the preparation of [pi]-conjugated redox-active thienyl oligomers and metal-mediated cross-coupling reactions. This is due to the presence of an electrochemically active thienyl heterocycle and a reactive dibromo­vinyl ...</p>
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<strong>Disciplines :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3A%22chemistry%2C+inorganic+%26+nuclear%22">chemistry, inorganic & nuclear</a>
<a href="https://search-data.ubfc.fr/search.php?s=discipline%3Acrystallography">crystallography</a>
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<div><strong>Collected date :</strong> from 2008 to 2009</div>
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<strong>Creators :</strong>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22S%C3%A9bastien+Cl%C3%A9ment%22">Sébastien Clément</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Prisca+Eckert%22">Prisca Eckert</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Laurent+Guyard%22">Laurent Guyard</a>
<a href="https://search-data.ubfc.fr/search.php?s=creator%3A%22Michael+Knorr%22">Michael Knorr</a>
...
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Attribution, Non Commercial, Share Alike