Literatura académica sobre el tema "Dioxazolone"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "Dioxazolone".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "Dioxazolone"
Borah, Gongutri, Preetismita Borah y Pitambar Patel. "Cp*Co(iii)-catalyzed ortho-amidation of azobenzenes with dioxazolones". Organic & Biomolecular Chemistry 15, n.º 18 (2017): 3854–59. http://dx.doi.org/10.1039/c7ob00540g.
Texto completoZhang, Lei, Xiangyun Zheng, Jinkang Chen, Kang Cheng, Licheng Jin, Xinpeng Jiang y Chuanming Yu. "Ru(ii)-Catalyzed C6-selective C–H amidation of 2-pyridones". Organic Chemistry Frontiers 5, n.º 20 (2018): 2969–73. http://dx.doi.org/10.1039/c8qo00795k.
Texto completoPan, Deng, Gen Luo, Yang Yu, Jimin Yang y Yi Luo. "Computational insights into Ir(iii)-catalyzed allylic C–H amination of terminal alkenes: mechanism, regioselectivity, and catalytic activity". RSC Advances 11, n.º 31 (2021): 19113–20. http://dx.doi.org/10.1039/d1ra03842g.
Texto completoHall, David S., Toren Hynes y J. R. Dahn. "Dioxazolone and Nitrile Sulfite Electrolyte Additives for Lithium-Ion Cells". Journal of The Electrochemical Society 165, n.º 13 (2018): A2961—A2967. http://dx.doi.org/10.1149/2.0341813jes.
Texto completoGauthier, Roby, David S. Hall, Katherine Lin, Jazmin Baltazar, Toren Hynes y J. R. Dahn. "Impact of Functionalization and Co-Additives on Dioxazolone Electrolyte Additives". Journal of The Electrochemical Society 167, n.º 8 (26 de mayo de 2020): 080540. http://dx.doi.org/10.1149/1945-7111/ab8ed6.
Texto completoGhosh, Payel, Sadhanendu Samanta y Alakananda Hajra. "Rhodium(iii)-catalyzed ortho-C–H amidation of 2-arylindazoles with a dioxazolone as an amidating reagent". Organic & Biomolecular Chemistry 18, n.º 9 (2020): 1728–32. http://dx.doi.org/10.1039/c9ob02756d.
Texto completoHande, Akshay Ekanath, Nachimuthu Muniraj y Kandikere Ramaiah Prabhu. "Cobalt(III)-Catalyzed C-H Amidation of Azobenzene Derivatives Using Dioxazolone as an Amidating Reagent". ChemistrySelect 2, n.º 21 (21 de julio de 2017): 5965–69. http://dx.doi.org/10.1002/slct.201701277.
Texto completoHande, Akshay Ekanath y 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, n.º 24 (28 de noviembre de 2017): 13405–13. http://dx.doi.org/10.1021/acs.joc.7b02500.
Texto completoLiu, Chen-Fei, Man Liu, Jun-Shu Sun, Chao Li y Lin Dong. "Synthesis of 2-aminobenzaldehydes by rhodium(iii)-catalyzed C–H amidation of aldehydes with dioxazolones". Organic Chemistry Frontiers 5, n.º 13 (2018): 2115–19. http://dx.doi.org/10.1039/c8qo00413g.
Texto completoTang, Shi-Biao, Xiao-Pan Fu, Gao-Rong Wu, Li-Li Zhang, Ke-Zuan Deng, Jin-Yue Yang, Cheng-Cai Xia y Ya-Fei Ji. "Rhodium(iii)-catalyzed C4-amidation of indole-oximes with dioxazolones via C–H activation". Organic & Biomolecular Chemistry 18, n.º 39 (2020): 7922–31. http://dx.doi.org/10.1039/d0ob01655a.
Texto completoTesis sobre el tema "Dioxazolone"
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.
Texto completoThis PhD work focus on the synthesis of polyurethanes through the in situ generation of isocyanates, using pathways with lower toxicity compared to the classical approach involving the direct use of isocyanates. The oxidative decarboxylation of oxamic acids leading to the formation of isocyanates was, first, carried out by thermal activation using a hypervalent iodine as an oxidant. A kinetic study on model reactions in the presence of alcohol, combined with computational modeling, notably revealed a catalytic effect of acetic acid, a by-product of the reaction, on the formation of urethane bonds. The CO2 generated by this reaction, leading to the formation of isocyanates, was then exploited for the synthesis of cross-linked polyurethane foams. The effects of various parameters, such as the nature of the monomers or the reaction temperature, on the morphology and properties of the obtained foams were thereafter studied. This activation reaction of oxamic acids was then carried out by light irradiation in the presence of a photocatalyst, allowing the production of polyurethane films. Modifying the components of the reaction mixture enabled the development of homogeneous formulations, particularly by changing the nature of the hypervalent iodine used. Finally, the synthesis of urethanes and polyurethanes from 1,4,2-dioxazol-5-ones was explored. After optimizing the catalytic conditions for generating isocyanates through the opening of these heterocycles, the generated CO2 was exploited for the production of polyurethane foams
Capítulos de libros sobre el tema "Dioxazolone"
"Imidazol-3-ium to 2H-1,3,4-Dioxazole". En Substance Index, editado por Backes, Fröhlich y Pedeken. Stuttgart: Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-114068.
Texto completo