Literatura científica selecionada sobre o tema "Oxidative alkenylation"
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Artigos de revistas sobre o assunto "Oxidative alkenylation"
Koubachi, Jamal, Nabil El Brahmi, Gérald Guillaumet e Saïd El Kazzouli. "Oxidative Alkenylation of Fused Bicyclic Heterocycles". European Journal of Organic Chemistry 2019, n.º 15 (1 de abril de 2019): 2568–86. http://dx.doi.org/10.1002/ejoc.201900199.
Texto completo da fonteSunke, Rajnikanth, Vimal Kumar, Mohd Ashraf Ashfaq, Swapna Yellanki, Raghavender Medisetti, Pushkar Kulkarni, E. V. Venkat Shivaji Ramarao, Nasreen Z. Ehtesham e Manojit Pal. "A Pd(ii)-catalyzed C–H activation approach to densely functionalized N-heteroaromatics related to neocryptolepine and their evaluation as potential inducers of apoptosis". RSC Advances 5, n.º 56 (2015): 44722–27. http://dx.doi.org/10.1039/c5ra06764b.
Texto completo da fonteCao, Hao, Dong Liu, Chao Liu, Xinquan Hu e Aiwen Lei. "Copper-catalyzed oxidative alkenylation of thioethers via Csp3–H functionalization". Organic & Biomolecular Chemistry 13, n.º 8 (2015): 2264–66. http://dx.doi.org/10.1039/c4ob02564d.
Texto completo da fonteTang, Jingjie, Mei Cong, Yi Xia, Gilles Quéléver, Yuting Fan, Fanqi Qu e Ling Peng. "Pd-catalyzed oxidative C–H alkenylation for synthesizing arylvinyltriazole nucleosides". Organic & Biomolecular Chemistry 13, n.º 1 (2015): 110–14. http://dx.doi.org/10.1039/c4ob01836b.
Texto completo da fonteMishra, Neeraj Kumar, Jihye Park, Satyasheel Sharma, Sangil Han, Mirim Kim, Youngmi Shin, Jinbong Jang, Jong Hwan Kwak, Young Hoon Jung e In Su Kim. "Direct access to isoindolines through tandem Rh(iii)-catalyzed alkenylation and cyclization of N-benzyltriflamides". Chem. Commun. 50, n.º 18 (2014): 2350–52. http://dx.doi.org/10.1039/c3cc49486a.
Texto completo da fonteKatsina, Tania, Elissavet E. Anagnostaki, Foteini Mitsa, Vasiliki Sarli e Alexandros L. Zografos. "Palladium-catalyzed direct alkenylation of 4-hydroxy-2-pyridones". RSC Advances 6, n.º 9 (2016): 6978–82. http://dx.doi.org/10.1039/c5ra26360c.
Texto completo da fonteMiyasaka, Mitsuru, Koji Hirano, Tetsuya Satoh e Masahiro Miura. "Palladium-Catalyzed Direct Oxidative Alkenylation of Azoles". Journal of Organic Chemistry 75, n.º 15 (6 de agosto de 2010): 5421–24. http://dx.doi.org/10.1021/jo101214y.
Texto completo da fonteZhu, Weihao, e T. Brent Gunnoe. "Advances in Rhodium-Catalyzed Oxidative Arene Alkenylation". Accounts of Chemical Research 53, n.º 4 (2 de abril de 2020): 920–36. http://dx.doi.org/10.1021/acs.accounts.0c00036.
Texto completo da fonteCao, Hua, Sai Lei, Jinqiang Liao, Jianping Huang, Huifang Qiu, Qinlin Chen, Shuxian Qiu e Yaoyi Chen. "Palladium(ii)-catalyzed intermolecular oxidative C-3 alkenylations of imidazo[1,2-a]pyridines by substrate-contolled regioselective C–H functionalization". RSC Adv. 4, n.º 91 (2014): 50137–40. http://dx.doi.org/10.1039/c4ra09669j.
Texto completo da fonteTang, Shan, Yong Wu, Wenqing Liao, Ruopeng Bai, Chao Liu e Aiwen Lei. "Revealing the metal-like behavior of iodine: an iodide-catalysed radical oxidative alkenylation". Chem. Commun. 50, n.º 34 (2014): 4496–99. http://dx.doi.org/10.1039/c4cc00644e.
Texto completo da fonteTeses / dissertações sobre o assunto "Oxidative alkenylation"
Nassiri, Sarah. "Fonctionnalisations régiosélectives de N-oxyde de pyrazolopyridines via des réactions de C-H activation pallado-catalysées". Electronic Thesis or Diss., Orléans, 2024. https://theses.univ-orleans.fr/prive/accesESR/2024ORLE1007_va.pdf.
Texto completo da fonteThe activation of C-H bonds has emerged as an attractive approach for advancing the synthesis of novel heterocyclic systems with potential applications across diverse fields, particularly in biology and pharmacy.The primary aim of this PhD thesis was to develop innovative strategies for the selective functionalization of nitrogen-containing heterocycles through C-H activation reactions, employing transition metal catalysis.In the first part, we developed a synthesis methodology enabling the regioselective functionalization at the ortho position of the N-oxide function in 7-azaindazole derivatives. The reaction goes through anoxidative arylation reaction, with various arenes and heteroarenes as coupling partners. This approachenables precise control over the position of functionalization through optimized reaction conditions, which is crucial to design new compounds with enhanced properties whatever the domains of application.In the second part of our research, we conducted a series of experiments to perform a regioselectiveoxidative alkenylation on the pyridine moiety of 4-azaindazole and 7-azaindazole. Using the N-oxidefunction as an ortho directing group allowed us to exert control over the position of functionalization.In the last part, we presented our work aimed at establishing optimal conditions for a direct arylation reaction on various 7-azaindazole analogues. The use of the N-oxide function favoured the regioselectivity of the reaction towards the C6 position
Keddie, Daniel Joseph. "The synthesis of novel profluorescent nitroxide probes". Thesis, Queensland University of Technology, 2008. https://eprints.qut.edu.au/16702/1/Daniel_Keddie_Thesis.pdf.
Texto completo da fonteKeddie, Daniel Joseph. "The synthesis of novel profluorescent nitroxide probes". Queensland University of Technology, 2008. http://eprints.qut.edu.au/16702/.
Texto completo da fontePrakash, Sekar, e 帕卡許. "Rhodium-Catalyzed Alkenylation and Cobalt-Catalyzed Oxidative Cyclization Reactions via C–H Bond Activation". Thesis, 2017. http://ndltd.ncl.edu.tw/handle/58qm33.
Texto completo da fonteCapítulos de livros sobre o assunto "Oxidative alkenylation"
Doba, Takahiro. "Iron-Catalyzed Oxidative C–H Alkenylation of Thiophenes with Enamines". In Springer Theses, 109–49. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-4121-6_5.
Texto completo da fonteLei, A., e S. Tang. "47.1.2.1.6 Alkyl-Mizoroki–Heck-Type Reactions". In Knowledge Updates 2023/1. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-147-00132.
Texto completo da fonte