Artigos de revistas sobre o tema "Oxidative alkenylation"
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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 fonteSingh, Keisham. "Recent Advances in C–H Bond Functionalization with Ruthenium-Based Catalysts". Catalysts 9, n.º 2 (12 de fevereiro de 2019): 173. http://dx.doi.org/10.3390/catal9020173.
Texto completo da fonteChen, Weiqiang, Hui-Jing Li, Qin-Ying Li e Yan-Chao Wu. "Direct oxidative coupling of N-acyl pyrroles with alkenes by ruthenium(ii)-catalyzed regioselective C2-alkenylation". Organic & Biomolecular Chemistry 18, n.º 3 (2020): 500–513. http://dx.doi.org/10.1039/c9ob02421b.
Texto completo da fonteQiu, Youai, Alexej Scheremetjew e Lutz Ackermann. "Electro-Oxidative C–C Alkenylation by Rhodium(III) Catalysis". Journal of the American Chemical Society 141, n.º 6 (12 de janeiro de 2019): 2731–38. http://dx.doi.org/10.1021/jacs.8b13692.
Texto completo da fonteLi, Jie, Christoph Kornhaaß e Lutz Ackermann. "Ruthenium-catalyzed oxidative C–H alkenylation of aryl carbamates". Chemical Communications 48, n.º 92 (2012): 11343. http://dx.doi.org/10.1039/c2cc36196e.
Texto completo da fonteJiao, Lin-Yu, e Martin Oestreich. "Oxidative Palladium(II)-Catalyzed C-7 Alkenylation of Indolines". Organic Letters 15, n.º 20 (8 de outubro de 2013): 5374–77. http://dx.doi.org/10.1021/ol402687t.
Texto completo da fonteKang, Dongjin, Jaeyoung Cho e Phil Ho Lee. "Palladium-catalyzed direct C-3 oxidative alkenylation of phosphachromones". Chemical Communications 49, n.º 89 (2013): 10501. http://dx.doi.org/10.1039/c3cc45874a.
Texto completo da fonteMiyasaka, Mitsuru, Koji Hirano, Tetsuya Satoh e Masahiro Miura. "ChemInform Abstract: Palladium-Catalyzed Direct Oxidative Alkenylation of Azoles." ChemInform 41, n.º 50 (18 de novembro de 2010): no. http://dx.doi.org/10.1002/chin.201050131.
Texto completo da fonteLah, Hafiz Ul, Faheem Rasool e Syed Khalid Yousuf. "Palladium catalyzed C(sp2)–C(sp2) bond formation. A highly regio- and chemoselective oxidative Heck C-3 alkenylation of pyrones and pyridones". RSC Advances 5, n.º 96 (2015): 78958–61. http://dx.doi.org/10.1039/c5ra12631b.
Texto completo da fonteLi, Yu-An, Ge Wu e Jia Li. "Palladium-Catalyzed N-Alkenylation of N-Aryl Phosphoramidates with Alkenes". Molecules 28, n.º 11 (31 de maio de 2023): 4466. http://dx.doi.org/10.3390/molecules28114466.
Texto completo da fonteTian, Yunfei, Luping Zheng, Ying Chen, Yufei Li, Mengna Wang, Weijun Fu e Zejiang Li. "Ferrous Salt-Catalyzed Oxidative Alkenylation of Indoles: Facile Access to 3-Alkylideneindolin-2-Ones". Catalysts 13, n.º 6 (25 de maio de 2023): 930. http://dx.doi.org/10.3390/catal13060930.
Texto completo da fonteKang, Dongjin, Jaeyoung Cho e Phil Ho Lee. "ChemInform Abstract: Palladium-Catalyzed Direct C-3 Oxidative Alkenylation of Phosphachromones." ChemInform 45, n.º 11 (27 de fevereiro de 2014): no. http://dx.doi.org/10.1002/chin.201411200.
Texto completo da fonteJiao, Lin-Yu, e Martin Oestreich. "ChemInform Abstract: Oxidative Palladium(II)-Catalyzed C-7 Alkenylation of Indolines." ChemInform 45, n.º 13 (14 de março de 2014): no. http://dx.doi.org/10.1002/chin.201413114.
Texto completo da fonteLi, Jie, Christoph Kornhaass e Lutz Ackermann. "ChemInform Abstract: Ruthenium-Catalyzed Oxidative C-H Alkenylation of Aryl Carbamates." ChemInform 44, n.º 13 (18 de março de 2013): no. http://dx.doi.org/10.1002/chin.201313030.
Texto completo da fonteLu, Nan, Chengxia Miao e Xiaozheng Lan. "Theoretical investigation on Rh(III)-catalyzed switchable C–H alkenylation of enamide with enone and Rh(I)-catalyzed decarbonylative version of 1,2,3,4-tetrahydroquinoline with anhydride". Thermal Science and Engineering 7, n.º 1 (1 de julho de 2024): 6267. http://dx.doi.org/10.24294/tse.v7i1.6267.
Texto completo da fonteKim, Namhoon, Minsik Min e Sungwoo Hong. "Regioselective palladium(ii)-catalyzed aerobic oxidative Heck-type C3 alkenylation of sulfocoumarins". Organic Chemistry Frontiers 2, n.º 12 (2015): 1621–24. http://dx.doi.org/10.1039/c5qo00294j.
Texto completo da fonteLessi, Marco, Attilio Nania, Melania Pittari, Laura Lodone, Angela Cuzzola e Fabio Bellina. "Palladium-Catalyzed Dehydrogenative C-2 Alkenylation of 5-Arylimidazoles and Related Azoles with Styrenes". Catalysts 11, n.º 7 (23 de junho de 2021): 762. http://dx.doi.org/10.3390/catal11070762.
Texto completo da fonteBerteina-Raboin, Sabine, Jamal Koubachi, Abderrahim Mouaddib e Gérald Guillaumet. "Pd/Cu-Catalyzed Oxidative C-H Alkenylation of Imidazo[1,2-a]pyridines". Synthesis 2009, n.º 02 (12 de dezembro de 2008): 271–76. http://dx.doi.org/10.1055/s-0028-1083252.
Texto completo da fonteZhang, Guangling, Ziyuan Li, Yue Huang, Jinyi Xu, Xiaoming Wu e Hequan Yao. "Direct C3-alkenylation of pyridin-4(1H)-one via oxidative Heck coupling". Tetrahedron 69, n.º 3 (janeiro de 2013): 1115–19. http://dx.doi.org/10.1016/j.tet.2012.11.061.
Texto completo da fonteTang, Jingjie, Mei Cong, Yi Xia, Gilles Quelever, Yuting Fan, Fanqi Qu e Ling Peng. "ChemInform Abstract: Pd-Catalyzed Oxidative C-H Alkenylation for Synthesizing Arylvinyltriazole Nucleosides." ChemInform 46, n.º 21 (maio de 2015): no. http://dx.doi.org/10.1002/chin.201521235.
Texto completo da fonteSun, Peng, Jiaojiao Yang, Zirui Song, Yichao Cai, Yajie Liu, Chunxia Chen, Xin Chen e Jinsong Peng. "Copper-Mediated One-Pot Synthesis of Indoles through Sequential Hydroamination and Cross-Dehydrogenative Coupling Reaction". Synthesis 52, n.º 01 (5 de novembro de 2019): 75–84. http://dx.doi.org/10.1055/s-0039-1690240.
Texto completo da fonteSawant, Devesh, Ram Pardasani, Iqubal Singh, Gaurav Tulsyan e Kishor Abbagani. "Ruthenium-Catalyzed Oxidative C–H Bond Alkenylation of 2-Phenylimidazo[1,2-a]pyridine". Synlett 26, n.º 12 (21 de maio de 2015): 1671–76. http://dx.doi.org/10.1055/s-0034-1380746.
Texto completo da fonteKozhushkov, Sergei I., e Lutz Ackermann. "Ruthenium-catalyzed direct oxidative alkenylation of arenes through twofold C–H bond functionalization". Chem. Sci. 4, n.º 3 (2013): 886–96. http://dx.doi.org/10.1039/c2sc21524a.
Texto completo da fonteSuzuki, Yudai, Bo Sun, Tatsuhiko Yoshino, Motomu Kanai e Shigeki Matsunaga. "Cp∗Co(III)-catalyzed oxidative C–H alkenylation of benzamides with ethyl acrylate". Tetrahedron 71, n.º 26-27 (julho de 2015): 4552–56. http://dx.doi.org/10.1016/j.tet.2015.02.032.
Texto completo da fonteKannaboina, Prakash, K. Anil Kumar e Parthasarathi Das. "Site-Selective Intermolecular Oxidative C-3 Alkenylation of 7-Azaindoles at Room Temperature". Organic Letters 18, n.º 5 (4 de fevereiro de 2016): 900–903. http://dx.doi.org/10.1021/acs.orglett.5b03429.
Texto completo da fonteGraczyk, Karolina, Wenbo Ma e Lutz Ackermann. "Oxidative Alkenylation of Aromatic Esters by Ruthenium-Catalyzed Twofold C–H Bond Cleavages". Organic Letters 14, n.º 16 (31 de julho de 2012): 4110–13. http://dx.doi.org/10.1021/ol301759v.
Texto completo da fonteMeng, Lingkui, Kun Wu, Chao Liu e Aiwen Lei. "Palladium-catalysed aerobic oxidative Heck-type alkenylation of Csp3–H for pyrrole synthesis". Chemical Communications 49, n.º 52 (2013): 5853. http://dx.doi.org/10.1039/c3cc42307g.
Texto completo da fonteShi, Renyi, Lijun Lu, Hua Zhang, Borui Chen, Yuchen Sha, Chao Liu e Aiwen Lei. "Palladium/Copper-Catalyzed Oxidative CH Alkenylation/N-Dealkylative Carbonylation of Tertiary Anilines". Angewandte Chemie 125, n.º 40 (14 de agosto de 2013): 10776–79. http://dx.doi.org/10.1002/ange.201303911.
Texto completo da fonteVora, Harit U., Anthony P. Silvestri, Casper J. Engelin e Jin-Quan Yu. "Rhodium(II)-Catalyzed Nondirected Oxidative Alkenylation of Arenes: Arene Loading at One Equivalent". Angewandte Chemie 126, n.º 10 (30 de janeiro de 2014): 2721–24. http://dx.doi.org/10.1002/ange.201310539.
Texto completo da fonteVora, Harit U., Anthony P. Silvestri, Casper J. Engelin e Jin-Quan Yu. "Rhodium(II)-Catalyzed Nondirected Oxidative Alkenylation of Arenes: Arene Loading at One Equivalent". Angewandte Chemie International Edition 53, n.º 10 (30 de janeiro de 2014): 2683–86. http://dx.doi.org/10.1002/anie.201310539.
Texto completo da fonteShi, Renyi, Lijun Lu, Hua Zhang, Borui Chen, Yuchen Sha, Chao Liu e Aiwen Lei. "Palladium/Copper-Catalyzed Oxidative CH Alkenylation/N-Dealkylative Carbonylation of Tertiary Anilines". Angewandte Chemie International Edition 52, n.º 40 (14 de agosto de 2013): 10582–85. http://dx.doi.org/10.1002/anie.201303911.
Texto completo da fonteJadhav, Pankaj P., Nilesh M. Kahar e Sudam G. Dawande. "Ruthenium(II)-Catalyzed Highly Chemo- and Regioselective Oxidative C6 Alkenylation of Indole-7-carboxamides". Organic Letters 23, n.º 22 (1 de novembro de 2021): 8673–77. http://dx.doi.org/10.1021/acs.orglett.1c02948.
Texto completo da fonteAnastasiou, Ioannis, Francesco Ferlin, Orlando Viteritti, Stefano Santoro e Luigi Vaccaro. "Pd/C-catalyzed aerobic oxidative C–H alkenylation of arenes in γ-valerolactone (GVL)". Molecular Catalysis 513 (agosto de 2021): 111787. http://dx.doi.org/10.1016/j.mcat.2021.111787.
Texto completo da fonteMo, Juntae, Sujin Lim, Sangjune Park, Taekyu Ryu, Sanghyuck Kim e Phil Ho Lee. "Oxidative ortho-alkenylation of arylphosphine oxides by rhodium-catalyzed C–H bond twofold cleavage". RSC Advances 3, n.º 40 (2013): 18296. http://dx.doi.org/10.1039/c3ra43764g.
Texto completo da fonteSharma, Satyasheel, Sangil Han, Youngmi Shin, Neeraj Kumar Mishra, Hyunji Oh, Jihye Park, Jong Hwan Kwak, Beom Soo Shin, Young Hoon Jung e In Su Kim. "Rh-catalyzed oxidative C2-alkenylation of indoles with alkynes: unexpected cleavage of directing group". Tetrahedron Letters 55, n.º 19 (maio de 2014): 3104–7. http://dx.doi.org/10.1016/j.tetlet.2014.04.001.
Texto completo da fonteSuzuki, Yudai, Bo Sun, Tatsuhiko Yoshino, Motomu Kanai e Shigeki Matsunaga. "ChemInform Abstract: Cp*Co(III)-Catalyzed Oxidative C-H Alkenylation of Benzamides with Ethylacrylate." ChemInform 46, n.º 42 (outubro de 2015): no. http://dx.doi.org/10.1002/chin.201542066.
Texto completo da fonteKim, Namhoon, Minsik Min e Sungwoo Hong. "ChemInform Abstract: Regioselective Palladium(II)-Catalyzed Aerobic Oxidative Heck-Type C3 Alkenylation of Sulfocoumarins." ChemInform 47, n.º 12 (março de 2016): no. http://dx.doi.org/10.1002/chin.201612185.
Texto completo da fonteZhang, Guangling, Ziyuan Li, Yue Huang, Jinyi Xu, Xiaoming Wu e Hequan Yao. "ChemInform Abstract: Direct C3-Alkenylation of Pyridin-4(1H)-one via Oxidative Heck Coupling." ChemInform 44, n.º 22 (13 de maio de 2013): no. http://dx.doi.org/10.1002/chin.201322159.
Texto completo da fonteLaha, Joydev K., Rohan A. Bhimpuria e Gajanan B. Mule. "Site-Selective Oxidative C4 Alkenylation of (NH)-Pyrroles Bearing an Electron-Withdrawing C2 Group". ChemCatChem 9, n.º 6 (24 de fevereiro de 2017): 1092–96. http://dx.doi.org/10.1002/cctc.201601468.
Texto completo da fonteMartínez, Ángel Manu, Nuria Rodríguez, Ramón Gómez Arrayás e Juan C. Carretero. "Synthesis of alkylidene pyrrolo[3,4-b]pyridin-7-one derivatives via RhIII-catalyzed cascade oxidative alkenylation/annulation of picolinamides". Chem. Commun. 50, n.º 46 (2014): 6105–7. http://dx.doi.org/10.1039/c4cc02322f.
Texto completo da fonteKnight, Brian J., Jacob O. Rothbaum e Eric M. Ferreira. "The design of a readily attachable and cleavable molecular scaffold for ortho-selective C–H alkenylation of arene alcohols". Chemical Science 7, n.º 3 (2016): 1982–87. http://dx.doi.org/10.1039/c5sc03948g.
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