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 (April 1, 2011): 205–8. http://dx.doi.org/10.3184/174751911x13001124874111.

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Tu, Wangyang, Fanglong Yang, Guoji Xu, Jiangtao Chi, Zhiwei Liu, Wei Peng, Bing Hu, et al. "Discovery of Imidazoisoindole Derivatives as Highly Potent and Orally Active Indoleamine-2,3-dioxygenase Inhibitors." ACS Medicinal Chemistry Letters 10, no. 6 (June 3, 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 (March 1, 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 reduces the complexity of the soybean extract. The derivatization works equally well for other imidazolinone herbicide acids. Because imidazoisoindolediones have characteristic fragmentation patterns, they are useful for mass spectroscopic confirmation of suspected residues.
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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 (September 8, 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 (April 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 (December 9, 2020): 146–52. http://dx.doi.org/10.1021/acs.joc.0c01860.

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Cul, Armelle, Adam Daïch, Bernard Decroix, Gérard Sanz, and 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, no. 48 (November 2004): 11029–39. http://dx.doi.org/10.1016/j.tet.2004.07.107.

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Crescenzi, Cristina, Thomas Fuchss, Dimitri Ippoliti, Annunziata Langella, Antonia Di Mola, Antonio Massa, and Diego Rozzi. "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 (April 30, 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 (July 14, 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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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 de fonctionnalisation de façon orthogonale. L’imidazoisoindole, hétérocycle tricyclique composé d’un noyau imidazole, est une plateforme pharmacologique très intéressante et présente des liaisons C—H avec des propriétés très diverses, mais aucune méthodologie de fonctionnalisation tardive de ces structures n’a encore été répertoriée dans la littérature. Ces travaux de thèse s’inscrivent dans ce contexte et présentent, (I) fort de l’expérience passée du laboratoire, une méthodologie robuste de synthèse à grande échelle d’imidazoisoindoles diversement substitués par activation C—H intramoléculaire pallado-catalysée ; (II) une extension des méthodologies standards de fonctionnalisation directe C2—H régiosélective de la série des 1,3-diazoles aux imidazo[5,1-a]isoindoles par catalyse coopérative palladium(0)-cuivre(I) ; (III) une méthodologie de mono-fonctionnalisation directe C(sp³)—H pallado-catalysée de la position benzylique des imidazo[2,1-a]isoindoles ; (IV) une étude préliminaire de la régiosélectivité observée lors de la borylation directe C(sp²)—H irido-catalysée des imidazo[2,1-a]isoindoles
For several decades, chemists constantly seek to push the limits of synthetic strategies by developing ever more efficient and more economical methodologies. In this context, transition metal-catalyzed direct functionalization of C—H bonds is one of the most powerful tools for constructing and funtionalizing simple molecules and ever more complex moieties, with a great diversity of C—H bonds. These strategies also answer the needs for the opening of the chemical space of functionalization. Imidazoisoindole, tricyclic heterocycle composed of an imidazole core, is a very interesting scaffold for biological activity and presents C—H bonds with very diverse properties, but late-functionalization methodology of these structures has yet to be listed in the literature. This work takes place in this context and presents, (I) based on past laboratory experience, a robust methodology to synthetize diversely substituted imidazoisoindoles at high scale by palladium-catalyzed intramolecular C—H activation ; (II) an extension of standard directC2—H functionalization of 1,3-diazole moieties applied to imidazo[5,1-a]isoindoles with a palladium(0)-copper(I) cooperative catalysis ; (III) a new methodology of direct C(sp³)—H palladium-catalyzed mono-functionalization at benzylic position of imidazo[2,1-a]isoindoles ; (IV) a preliminary study of the observed regioselectivity of iridium-catalyzed direct C(sp²)—H borylation of imidazo[2,1-a]isoindoles
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