Academic literature on the topic 'Imidazoisoindoles'

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Journal articles on the topic "Imidazoisoindoles"

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Alya, Ashraf. "Facile synthesis of imidazoisoindolones and quinoxalinediones from 2,3-diamino-1,4-naphthoquinone." Journal of Chemical Research 35, no. 4 (2011): 205–8. http://dx.doi.org/10.3184/174751911x13001124874111.

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Tu, Wangyang, Fanglong Yang, Guoji Xu, et al. "Discovery of Imidazoisoindole Derivatives as Highly Potent and Orally Active Indoleamine-2,3-dioxygenase Inhibitors." ACS Medicinal Chemistry Letters 10, no. 6 (2019): 949–53. http://dx.doi.org/10.1021/acsmedchemlett.9b00114.

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Mortimer, Richard D., and Dorcas F. Weber. "Determination of Residual Imazethapyr in Soybeans by Gas Chromatography/Nitrogen-Phosphorus Detection." Journal of AOAC INTERNATIONAL 76, no. 2 (1993): 377–81. http://dx.doi.org/10.1093/jaoac/76.2.377.

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Abstract Imazethapyr, a recently introduced imidazolinone herbicide, is registered for use on soybeans and other legumes in the United States and Canada. Its maximum allowed residue level in soybeans is 0.1 ppm. A method was developed to allow the measurement of ≥0.01 ppm imazethapyr on soybeans. The method exploits the ready cyclization of the nonvolatile acid to the volatile imidazoisoindol-3,5-dione by using an excess of easily removed, watersoluble carbodiimide and the selectivity of gas chromatography with nitrogen-phosphorus detection. A simple cleanup on a diol-bonded silica minicolumn
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Aly, Ashraf A. "ChemInform Abstract: Facile Synthesis of Imidazoisoindolones and Quinoxalinediones from 2,3-Diamino-1,4-naphthoquinone." ChemInform 42, no. 40 (2011): no. http://dx.doi.org/10.1002/chin.201140166.

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Dandepally, Srinivasa Reddy, and Alfred L. Williams. "Synthesis of imidazoisoindol-3-ones by a palladium-catalyzed intramolecular C–H insertion reaction." Tetrahedron Letters 50, no. 13 (2009): 1395–98. http://dx.doi.org/10.1016/j.tetlet.2009.01.019.

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Ahmadi, Fereshteh, Hamid Reza Goli, Yaser Balmohammadi, and Ayoob Bazgir. "Isocyanide Insertion–Cyclization Reaction for Imidazoisoindol-5-imine Scaffold Synthesis: A Selective Solvatochromic Fluorescent Probe for Methanol Detection." Journal of Organic Chemistry 86, no. 1 (2020): 146–52. http://dx.doi.org/10.1021/acs.joc.0c01860.

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Cul, Armelle, Adam Daïch, Bernard Decroix, Gérard Sanz та Luc Van Hijfte. "Kinetic versus thermodynamic access to imidazoisoindolones, benzimidazoisoindolones, and [1,4]diazepinoisoindolones: intramolecular nitrogen and π-aromatic trapping of N-acyliminium cation". Tetrahedron 60, № 48 (2004): 11029–39. http://dx.doi.org/10.1016/j.tet.2004.07.107.

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Crescenzi, Cristina, Thomas Fuchss, Dimitri Ippoliti, et al. "Reiterative Chiral Resolution/Racemization/Recycle (RRR Synthesis) for an Effective and Scalable Process for the Enantioselective Synthesis of a Dual IDO1/TDO2 Inhibitor Imidazoisoindole Derivative." Organic Process Research & Development 24, no. 6 (2020): 1018–23. http://dx.doi.org/10.1021/acs.oprd.0c00004.

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Dandepally, Srinivasa Reddy, and Alfred L. Williams. "ChemInform Abstract: Synthesis of Imidazoisoindol-3-ones by a Palladium-Catalyzed Intramolecular C-H Insertion Reaction." ChemInform 40, no. 28 (2009). http://dx.doi.org/10.1002/chin.200928107.

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Dissertations / Theses on the topic "Imidazoisoindoles"

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Panza, Florian. "Fοnctiοnnalisatiοn directe οrthοgοnale métallο-catalysée des sites carbοne-hydrοgène des platefοrmes pharmacοlοgiques à cοeur imidazοisοindοle". Electronic Thesis or Diss., Normandie, 2024. http://www.theses.fr/2024NORMIR11.

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Abstract:
Depuis quelques décennies, les chimistes cherchent à toujours repousser les limites des stratégies de synthèse en développant des méthodologies toujours plus efficaces, plus simples et plus économes. Dans ce contexte, la fonctionnalisation directe de liaisons C—H catalysée par des métaux de transition constitue l’un des outils les plus puissants pour construire et fonctionnaliser des molécules simples mais aussi des édifices moléculaires de plus en plus complexes, avec une grande diversité de liaisons C—H, ces stratégies répondant également aux besoins actuels d’ouverture de l’espace chimique
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