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Academic literature on the topic 'Imidazoisoindoles'
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Journal articles on the topic "Imidazoisoindoles"
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.
Full textTu, 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.
Full textMortimer, 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.
Full textAly, 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.
Full textDandepally, 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.
Full textAhmadi, 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.
Full textCul, 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.
Full textCrescenzi, 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.
Full textDandepally, 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.
Full textDissertations / Theses on the topic "Imidazoisoindoles"
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.
Full textFor 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