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Artykuły w czasopismach na temat "Imidazoisoindoles"
Alya, Ashraf. "Facile synthesis of imidazoisoindolones and quinoxalinediones from 2,3-diamino-1,4-naphthoquinone". Journal of Chemical Research 35, nr 4 (1.04.2011): 205–8. http://dx.doi.org/10.3184/174751911x13001124874111.
Pełny tekst źródłaTu, Wangyang, Fanglong Yang, Guoji Xu, Jiangtao Chi, Zhiwei Liu, Wei Peng, Bing Hu i in. "Discovery of Imidazoisoindole Derivatives as Highly Potent and Orally Active Indoleamine-2,3-dioxygenase Inhibitors". ACS Medicinal Chemistry Letters 10, nr 6 (3.06.2019): 949–53. http://dx.doi.org/10.1021/acsmedchemlett.9b00114.
Pełny tekst źródłaMortimer, Richard D., i Dorcas F. Weber. "Determination of Residual Imazethapyr in Soybeans by Gas Chromatography/Nitrogen-Phosphorus Detection". Journal of AOAC INTERNATIONAL 76, nr 2 (1.03.1993): 377–81. http://dx.doi.org/10.1093/jaoac/76.2.377.
Pełny tekst źródłaAly, Ashraf A. "ChemInform Abstract: Facile Synthesis of Imidazoisoindolones and Quinoxalinediones from 2,3-Diamino-1,4-naphthoquinone." ChemInform 42, nr 40 (8.09.2011): no. http://dx.doi.org/10.1002/chin.201140166.
Pełny tekst źródłaDandepally, Srinivasa Reddy, i Alfred L. Williams. "Synthesis of imidazoisoindol-3-ones by a palladium-catalyzed intramolecular C–H insertion reaction". Tetrahedron Letters 50, nr 13 (kwiecień 2009): 1395–98. http://dx.doi.org/10.1016/j.tetlet.2009.01.019.
Pełny tekst źródłaAhmadi, Fereshteh, Hamid Reza Goli, Yaser Balmohammadi i 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, nr 1 (9.12.2020): 146–52. http://dx.doi.org/10.1021/acs.joc.0c01860.
Pełny tekst źródłaCul, Armelle, Adam Daïch, Bernard Decroix, Gérard Sanz i 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, nr 48 (listopad 2004): 11029–39. http://dx.doi.org/10.1016/j.tet.2004.07.107.
Pełny tekst źródłaCrescenzi, Cristina, Thomas Fuchss, Dimitri Ippoliti, Annunziata Langella, Antonia Di Mola, Antonio Massa i 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, nr 6 (30.04.2020): 1018–23. http://dx.doi.org/10.1021/acs.oprd.0c00004.
Pełny tekst źródłaDandepally, Srinivasa Reddy, i Alfred L. Williams. "ChemInform Abstract: Synthesis of Imidazoisoindol-3-ones by a Palladium-Catalyzed Intramolecular C-H Insertion Reaction." ChemInform 40, nr 28 (14.07.2009). http://dx.doi.org/10.1002/chin.200928107.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaFor 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