Bibliografias temáticas / Dioxazolone

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Literatura científica selecionada sobre o tema "Dioxazolone"

Autor: Grafiati
Publicado: 19 de outubro de 2024
Última modificação: 31 de julho de 2025

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Artigos de revistas sobre o assunto "Dioxazolone"

1

Borah, Gongutri, Preetismita Borah, and Pitambar Patel. "Cp*Co(iii)-catalyzed ortho-amidation of azobenzenes with dioxazolones." Organic & Biomolecular Chemistry 15, no. 18 (2017): 3854–59. http://dx.doi.org/10.1039/c7ob00540g.

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2

Zhang, Lei, Xiangyun Zheng, Jinkang Chen, et al. "Ru(ii)-Catalyzed C6-selective C–H amidation of 2-pyridones." Organic Chemistry Frontiers 5, no. 20 (2018): 2969–73. http://dx.doi.org/10.1039/c8qo00795k.

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3

Pan, Deng, Gen Luo, Yang Yu, Jimin Yang, and Yi Luo. "Computational insights into Ir(iii)-catalyzed allylic C–H amination of terminal alkenes: mechanism, regioselectivity, and catalytic activity." RSC Advances 11, no. 31 (2021): 19113–20. http://dx.doi.org/10.1039/d1ra03842g.

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DFT studies on Ir(iii)-catalyzed branch-selective allylic C–H amination of terminal olefins with methyl dioxazolone have been carried out to investigate the mechanism, including the origins of regioselectivity and catalytic activity difference.
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4

Hall, David S., Toren Hynes, and J. R. Dahn. "Dioxazolone and Nitrile Sulfite Electrolyte Additives for Lithium-Ion Cells." Journal of The Electrochemical Society 165, no. 13 (2018): A2961—A2967. http://dx.doi.org/10.1149/2.0341813jes.

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5

Gauthier, Roby, David S. Hall, Katherine Lin, Jazmin Baltazar, Toren Hynes, and J. R. Dahn. "Impact of Functionalization and Co-Additives on Dioxazolone Electrolyte Additives." Journal of The Electrochemical Society 167, no. 8 (2020): 080540. http://dx.doi.org/10.1149/1945-7111/ab8ed6.

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6

Ghosh, Payel, Sadhanendu Samanta, and Alakananda Hajra. "Rhodium(iii)-catalyzed ortho-C–H amidation of 2-arylindazoles with a dioxazolone as an amidating reagent." Organic & Biomolecular Chemistry 18, no. 9 (2020): 1728–32. http://dx.doi.org/10.1039/c9ob02756d.

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A simple and efficient method for directed amidation of a wide range of 2-arylindazoles has been established for the first time through a rhodium-catalyzed C–H activation reaction with alkyl, aryl and heteroaryl dioxazolones.
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7

Hande, Akshay Ekanath, Nachimuthu Muniraj, and Kandikere Ramaiah Prabhu. "Cobalt(III)-Catalyzed C-H Amidation of Azobenzene Derivatives Using Dioxazolone as an Amidating Reagent." ChemistrySelect 2, no. 21 (2017): 5965–69. http://dx.doi.org/10.1002/slct.201701277.

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Hande, Akshay Ekanath, and Kandikere Ramaiah Prabhu. "Ru(II)-Catalyzed C–H Amidation of Indoline at the C7-Position Using Dioxazolone as an Amidating Agent: Synthesis of 7-Amino Indoline Scaffold." Journal of Organic Chemistry 82, no. 24 (2017): 13405–13. http://dx.doi.org/10.1021/acs.joc.7b02500.

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9

Lee, Seungmin, Minsuk Kim, Hyewon Han, and Jongwoo Son. "Dioxazolones as electrophilic amide sources in copper-catalyzed and -mediated transformations." Beilstein Journal of Organic Chemistry 21 (January 22, 2025): 200–216. https://doi.org/10.3762/bjoc.21.12.

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Over the past decade, dioxazolones have been widely used as N-acylamide sources in amidation processes of challenging substrates, typically employing precious transition metals. However, these catalytic systems often present several challenges associated with cost, toxicity, stability, and recyclability. Among the 3d transition metals, copper catalysts have been gaining increasing attention owing to their abundance, cost-effectiveness, and sustainability. Recently, these catalytic systems have been applied to the chemical transformation of dioxazolones, conferring a convenient protocol towards
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10

Liu, Chen-Fei, Man Liu, Jun-Shu Sun, Chao Li, and Lin Dong. "Synthesis of 2-aminobenzaldehydes by rhodium(iii)-catalyzed C–H amidation of aldehydes with dioxazolones." Organic Chemistry Frontiers 5, no. 13 (2018): 2115–19. http://dx.doi.org/10.1039/c8qo00413g.

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Mais fontes

Teses / dissertações sobre o assunto "Dioxazolone"

1

Jaussaud, Quentin. "Génération in situ d’isocyanates par décarboxylation d’acides oxamiques pour l’élaboration de matériaux polyuréthanes." Electronic Thesis or Diss., Bordeaux, 2024. http://www.theses.fr/2024BORD0139.

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Ces travaux de thèse portent sur la synthèse de polyuréthanes par génération in situ d’isocyanates, à travers différentes voies de moindre toxicité que la voie classique faisant appel à l’utilisation directe d’isocyanates. Dans un premier temps, la décarboxylation oxydante des acides oxamiques conduisant à la formation d’isocyanates a été réalisée par activation thermique grâce à l’utilisation d’un iodure hypervalent, jouant le rôle d’oxydant. Une étude cinétique sur des réactions modèles en présence d’alcool, associé à une modélisation numérique, ont notamment mis en évidence un effet catalyt
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Capítulos de livros sobre o assunto "Dioxazolone"

1

"Imidazol-3-ium to 2H-1,3,4-Dioxazole." In Substance Index, edited by Backes, Fröhlich, and Pedeken. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-114068.

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