Eric Deniau
Professeur des universités
CNU : SECTION 32 - Chimie organique, minerale, industrielle
Laboratoire / équipe
Publications
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"citationFull_s":"Nathan Martin, Aurélien Moncomble, Lydie Pélinski, Eric Deniau, Till Bousquet. Base‐ and Visible‐Light‐Promoted Formation of 3‐Benzyl‐3‐Methoxyisoindolin‐1‐one. <i>European Journal of Organic Chemistry</i>, 2024, Eur. J. Org. Chem., 27 (18), pp.e202400025. <a target=\"_blank\" href=\"https://dx.doi.org/10.1002/ejoc.202400025\">⟨10.1002/ejoc.202400025⟩</a>. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-04625222v1\">⟨hal-04625222⟩</a>",
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"citationRef_s":"<i>ACS Omega</i>, 2023, Acs Omega, 8 (25), pp.23067-23077. <a target=\"_blank\" href=\"https://dx.doi.org/10.1021/acsomega.3c02362\">⟨10.1021/acsomega.3c02362⟩</a>",
"citationFull_s":"H. Jellali, N. Amri, Y. E. Mukhrish, I. S. Al Nasr, W. S. Koko, et al.. Copper-Catalyzed Asymmetric Hydroboration Reaction of Novel Methylene Isoindolinone Compounds through Microwave Irradiation and Their Antileishmanial and Antitoxoplasma Activities. <i>ACS Omega</i>, 2023, Acs Omega, 8 (25), pp.23067-23077. <a target=\"_blank\" href=\"https://dx.doi.org/10.1021/acsomega.3c02362\">⟨10.1021/acsomega.3c02362⟩</a>. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-04273129v1\">⟨hal-04273129⟩</a>",
"title_s":["Copper-Catalyzed Asymmetric Hydroboration Reaction of Novel Methylene Isoindolinone Compounds through Microwave Irradiation and Their Antileishmanial and Antitoxoplasma Activities"],
"authFullName_s":["H. Jellali","N. Amri","Y. E. Mukhrish","I. S. Al Nasr","W. S. Koko","T. A. Khan","Eric Deniau","Mathieu Sauthier","H. Ghalla","N. Hamdi"],
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"citationRef_s":"<i>Creating New Bonds in Physical Organic chemistry</i>, Nov 2022, Fréjus, France",
"citationFull_s":"Nathan Martin, Aurélien Moncomble, Lydie Pelinski, Till Bousquet, Eric Deniau. Formation d’isoindolinones à partir de sels de diazoniums. <i>Creating New Bonds in Physical Organic chemistry</i>, Nov 2022, Fréjus, France. <a target=\"_blank\" href=\"https://hal.science/hal-03933629v1\">⟨hal-03933629⟩</a>",
"title_s":["Formation d’isoindolinones à partir de sels de diazoniums"],
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"citationFull_s":"Nathan Martin, Till Bousquet, Lydie Pelinski, Eric Deniau. New Photo-Induced Alkoxyarylation of 3-Methylene Isoindolinones Using Aryl Diazonium Salts. <i>Journées de la Chimie Organique</i>, Nov 2022, Palaiseau, France. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-04160138v1\">⟨hal-04160138⟩</a>",
"title_s":["New Photo-Induced Alkoxyarylation of 3-Methylene Isoindolinones Using Aryl Diazonium Salts"],
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"citationRef_s":"<i>Polycyclic Aromatic Compounds</i>, 2022, Polycyclic Aromatic Compounds, 42 (4), pp.1806-1813. <a target=\"_blank\" href=\"https://dx.doi.org/10.1080/10406638.2020.1809468\">⟨10.1080/10406638.2020.1809468⟩</a>",
"citationFull_s":"Hamida Jelali, Lamjed Mansour, Eric Deniau, Mathieu Sauthier, Naceur Hamdi. An efficient synthesis of phthalimides and their biological activities. <i>Polycyclic Aromatic Compounds</i>, 2022, Polycyclic Aromatic Compounds, 42 (4), pp.1806-1813. <a target=\"_blank\" href=\"https://dx.doi.org/10.1080/10406638.2020.1809468\">⟨10.1080/10406638.2020.1809468⟩</a>. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-04303213v1\">⟨hal-04303213⟩</a>",
"title_s":["An efficient synthesis of phthalimides and their biological activities"],
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"citationFull_s":"Hamida Jelali, Lamjed Mansour, Jameel Al-Tamimi, Eric Deniau, Mathieu Sauthier, et al.. Synthesis and Characterization of 3-Methylene Isoindolinones by Two Synthetic Routes. <i>Polycyclic Aromatic Compounds</i>, 2021, Polycyclic Aromatic Compounds, pp.1-13. <a target=\"_blank\" href=\"https://dx.doi.org/10.1080/10406638.2021.1971269\">⟨10.1080/10406638.2021.1971269⟩</a>. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-04548244v1\">⟨hal-04548244⟩</a>",
"title_s":["Synthesis and Characterization of 3-Methylene Isoindolinones by Two Synthetic Routes"],
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"citationFull_s":"Tiphaine Dedours, Hamida Jelali, Stephane Lebrun, Mathieu Sauthier, Eric Deniau. Hydrofonctionnalisation de 3-méthylène isoindolinones métallo-catalysée. Application à la synthèse de molécules anti-bactériennes. <i>Journées Nord Ouest Européennes des Jeunes Chercheurs (JNOEJC) 2019</i>, Jun 2019, Mont Saint Aignan, France. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-03509952v1\">⟨hal-03509952⟩</a>",
"title_s":["Hydrofonctionnalisation de 3-méthylène isoindolinones métallo-catalysée. Application à la synthèse de molécules anti-bactériennes"],
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"citationFull_s":"Fabien Gelat, Michaël Coffinet, Stephane Lebrun, Francine Agbossou-Niedercorn, Christophe Michon, et al.. Total synthesis of (-)-herbaric acid. Organocatalyzed asymmetric halolactonization of acrylate-type carboxylic acids. <i>9ème Symposium Francophone de Synthèse Totale (SFST)</i>, May 2019, Nantes, France. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-03509948v1\">⟨hal-03509948⟩</a>",
"title_s":["Total synthesis of (-)-herbaric acid. Organocatalyzed asymmetric halolactonization of acrylate-type carboxylic acids"],
"authFullName_s":["Fabien Gelat","Michaël Coffinet","Stephane Lebrun","Francine Agbossou-Niedercorn","Christophe Michon","Eric Deniau"],
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"citationFull_s":"Hamida Jelali, Stephane Lebrun, Mathieu Sauthier, Eric Deniau. Hydro-fonctionnalisation métallo-catalysée d’énamides. Application à la synthèse de molécules antibactériennes. <i>Journées des Doctorants</i>, Mar 2019, Villeneuve d'Ascq, France. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-03509386v1\">⟨hal-03509386⟩</a>",
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"title_s":["Nouveaux développements méthodologiques en organo-photocatalyse. Application à la synthèse de produits naturels et/ou biologiquement actifs"],
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"title_s":["Nouveaux développements méthodologiques en organo-photocatalyse. Application à la synthèse de molécules naturelles et/ou biologiquement actives"],
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"title_s":["Hydroboration asymétrique d’énamides catalysée au cuivre. Application à la synthèse de nouveaux dérivés aminoborés énantioenrichis"],
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"citationFull_s":"Romain Sallio, Stephane Lebrun, Frederic Capet, Francine Agbossou-Niedercorn, Christophe Michon, et al.. Stereoselective organocatalyzed intramolecular aza-Michael reaction for the preparation of 3-substituted isoindolinones. Application to the synthesis of a new pazinaclone analogue. <i>Journées Nord Ouest Européennes des Jeunes Chercheurs (JNOEJC) 2018</i>, Jun 2018, Villeneuve d'Ascq, France. <a target=\"_blank\" href=\"https://lilloa.hal.science/hal-03509924v1\">⟨hal-03509924⟩</a>",
"title_s":["Stereoselective organocatalyzed intramolecular aza-Michael reaction for the preparation of 3-substituted isoindolinones. Application to the synthesis of a new pazinaclone analogue"],
"authFullName_s":["Romain Sallio","Stephane Lebrun","Frederic Capet","Francine Agbossou-Niedercorn","Christophe Michon","Eric Deniau"],
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"title_s":["Nouveaux développements méthodologiques en organo-photocatalyse. Application à la synthèse de produits naturels et/ou biologiquement actifs"],
"authFullName_s":["Tiphaine Dedours","Nicolas Demarles","Stephane Lebrun","Eric Deniau"],
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"title_s":["Nouveaux développements méthodologiques en organo-photocatalyse. Application à la synthèse de produits naturels et/ou biologiquement actifs"],
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"citationRef_s":"<i>Beilstein Journal of Organic Chemistry</i>, 2018, 14, pp.593-602. <a target=\"_blank\" href=\"https://dx.doi.org/10.3762/bjoc.14.46\">⟨10.3762/bjoc.14.46⟩</a>",
"citationFull_s":"Romain Sallio, Stéphane Lebrun, Frédéric Capet, Francine Agbossou-Niedercorn, Christophe Michon, et al.. Diastereoselective auxiliary- and catalyst-controlled intramolecular aza-Michael reaction for the elaboration of enantioenriched 3-substituted isoindolinones. Application to the synthesis of a new pazinaclone analogue. <i>Beilstein Journal of Organic Chemistry</i>, 2018, 14, pp.593-602. <a target=\"_blank\" href=\"https://dx.doi.org/10.3762/bjoc.14.46\">⟨10.3762/bjoc.14.46⟩</a>. <a target=\"_blank\" href=\"https://hal.science/hal-01786976v2\">⟨hal-01786976v2⟩</a>",
"title_s":["Diastereoselective auxiliary- and catalyst-controlled intramolecular aza-Michael reaction for the elaboration of enantioenriched 3-substituted isoindolinones. Application to the synthesis of a new pazinaclone analogue"],
"authFullName_s":["Romain Sallio","Stéphane Lebrun","Frédéric Capet","Francine Agbossou-Niedercorn","Christophe Michon","Eric Deniau"],
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"citationRef_s":"<i>SYNLETT</i>, 2017, 28 (02), pp.225 - 230. <a target=\"_blank\" href=\"https://dx.doi.org/10.1055/s-0036-1588895\">⟨10.1055/s-0036-1588895⟩</a>",
"citationFull_s":"Fabien Gelat, Stéphane Lebrun, Natacha Henry, Francine Agbossou-Niedercorn, Christophe Michon, et al.. Total Synthesis of (–)-Herbaric Acid through Organocatalyzed Asymmetric Halolactonization of Acrylate-Type Benzoic Acids. <i>SYNLETT</i>, 2017, 28 (02), pp.225 - 230. <a target=\"_blank\" href=\"https://dx.doi.org/10.1055/s-0036-1588895\">⟨10.1055/s-0036-1588895⟩</a>. <a target=\"_blank\" href=\"https://hal.science/hal-01663144v1\">⟨hal-01663144⟩</a>",
"title_s":["Total Synthesis of (–)-Herbaric Acid through Organocatalyzed Asymmetric Halolactonization of Acrylate-Type Benzoic Acids"],
"authFullName_s":["Fabien Gelat","Stéphane Lebrun","Natacha Henry","Francine Agbossou-Niedercorn","Christophe Michon","Eric Deniau"],
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"citationRef_s":"<i>Tetrahedron: Asymmetry</i>, 2016, 27 (19), pp.980 - 989. <a target=\"_blank\" href=\"https://dx.doi.org/10.1016/j.tetasy.2016.07.010\">⟨10.1016/j.tetasy.2016.07.010⟩</a>",
"citationFull_s":"Fabien Gelat, Michaël Coffinet, Stéphane Lebrun, Francine Agbossou-Niedercorn, Christophe Michon, et al.. Regioselective organocatalyzed asymmetric bromolactonization of aryl acrylate-type carboxylic acids: a new approach towards enantioenriched 3-substituted isobenzofuranones. <i>Tetrahedron: Asymmetry</i>, 2016, 27 (19), pp.980 - 989. <a target=\"_blank\" href=\"https://dx.doi.org/10.1016/j.tetasy.2016.07.010\">⟨10.1016/j.tetasy.2016.07.010⟩</a>. <a target=\"_blank\" href=\"https://hal.science/hal-01663146v1\">⟨hal-01663146⟩</a>",
"title_s":["Regioselective organocatalyzed asymmetric bromolactonization of aryl acrylate-type carboxylic acids: a new approach towards enantioenriched 3-substituted isobenzofuranones"],
"authFullName_s":["Fabien Gelat","Michaël Coffinet","Stéphane Lebrun","Francine Agbossou-Niedercorn","Christophe Michon","Eric Deniau"],
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"citationRef_s":"<i>European Journal of Organic Chemistry</i>, 2015, 2015 (9), pp.1995 - 2004. <a target=\"_blank\" href=\"https://dx.doi.org/10.1002/ejoc.201403573\">⟨10.1002/ejoc.201403573⟩</a>",
"citationFull_s":"Stéphane Lebrun, Romain Sallio, Mélanie Dubois, Francine Agbossou-Niedercorn, Eric Deniau, et al.. Chiral Phase-Transfer-Catalyzed Intramolecular aza-Michael Reactions for the Asymmetric Synthesis of Isoindolinones. <i>European Journal of Organic Chemistry</i>, 2015, 2015 (9), pp.1995 - 2004. <a target=\"_blank\" href=\"https://dx.doi.org/10.1002/ejoc.201403573\">⟨10.1002/ejoc.201403573⟩</a>. <a target=\"_blank\" href=\"https://hal.science/hal-01663153v1\">⟨hal-01663153⟩</a>",
"title_s":["Chiral Phase-Transfer-Catalyzed Intramolecular aza-Michael Reactions for the Asymmetric Synthesis of Isoindolinones"],
"authFullName_s":["Stéphane Lebrun","Romain Sallio","Mélanie Dubois","Francine Agbossou-Niedercorn","Eric Deniau","Christophe Michon"],
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"citationFull_s":"Romain Sallio, Stéphane Lebrun, Eric Deniau. A new asymmetric synthesis of 2,6-cis-diarylated piperidines. <i>Tetrahedron: Asymmetry</i>, 2015, 26 (4), pp.209 - 213. <a target=\"_blank\" href=\"https://dx.doi.org/10.1016/j.tetasy.2014.12.010\">⟨10.1016/j.tetasy.2014.12.010⟩</a>. <a target=\"_blank\" href=\"https://hal.science/hal-01663154v1\">⟨hal-01663154⟩</a>",
"title_s":["A new asymmetric synthesis of 2,6-cis-diarylated piperidines"],
"authFullName_s":["Romain Sallio","Stéphane Lebrun","Eric Deniau"],
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"citationRef_s":"<i>European Journal of Organic Chemistry</i>, 2014, 2014 (20), pp.4381 - 4388. <a target=\"_blank\" href=\"https://dx.doi.org/10.1002/ejoc.201402202\">⟨10.1002/ejoc.201402202⟩</a>",
"citationFull_s":"Romain Sallio, Stéphane Lebrun, Nicolas Gigant, Isabelle Gillaizeau, Eric Deniau. Asymmetric Synthesis of 2-Heteroaryl Cyclic Amines: Total Synthesis of (-)-Anabasine. <i>European Journal of Organic Chemistry</i>, 2014, 2014 (20), pp.4381 - 4388. <a target=\"_blank\" href=\"https://dx.doi.org/10.1002/ejoc.201402202\">⟨10.1002/ejoc.201402202⟩</a>. <a target=\"_blank\" href=\"https://hal.science/hal-01663155v1\">⟨hal-01663155⟩</a>",
"title_s":["Asymmetric Synthesis of 2-Heteroaryl Cyclic Amines: Total Synthesis of (-)-Anabasine"],
"authFullName_s":["Romain Sallio","Stéphane Lebrun","Nicolas Gigant","Isabelle Gillaizeau","Eric Deniau"],
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