Статті в журналах з теми "Activation de la liaison C(sp2)-H"
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Wencel-Delord, Joanna, and Françoise Colobert. "Asymmetric C(sp2)H Activation." Chemistry - A European Journal 19, no. 42 (September 17, 2013): 14010–17. http://dx.doi.org/10.1002/chem.201302576.
Повний текст джерелаWencel-Delord, Joanna, and Francoise Colobert. "ChemInform Abstract: Asymmetric C(sp2)-H Activation." ChemInform 45, no. 2 (December 19, 2013): no. http://dx.doi.org/10.1002/chin.201402241.
Повний текст джерелаBakthadoss, Manickam, Tadiparthi Thirupathi Reddy, Vishal Agarwal, and Duddu S. Sharada. "Ester-directed orthogonal dual C–H activation and ortho aryl C–H alkenylation via distal weak coordination." Chemical Communications 58, no. 9 (2022): 1406–9. http://dx.doi.org/10.1039/d1cc06097j.
Повний текст джерелаDutta, Uttam, Sudip Maiti, Trisha Bhattacharya, and Debabrata Maiti. "Arene diversification through distal C(sp2)−H functionalization." Science 372, no. 6543 (May 13, 2021): eabd5992. http://dx.doi.org/10.1126/science.abd5992.
Повний текст джерелаZhang, Yanghui, Bo Zhou, and Ailan Lu. "Pd-Catalyzed C–H Silylation Reactions with Disilanes." Synlett 30, no. 06 (December 18, 2018): 685–93. http://dx.doi.org/10.1055/s-0037-1610339.
Повний текст джерелаBritton, Luke, Jamie H. Docherty, Andrew P. Dominey, and Stephen P. Thomas. "Iron-Catalysed C(sp2)-H Borylation Enabled by Carboxylate Activation." Molecules 25, no. 4 (February 18, 2020): 905. http://dx.doi.org/10.3390/molecules25040905.
Повний текст джерелаGeng, Cuihuan, Sujuan Zhang, Chonggang Duan, Tongxiang Lu, Rongxiu Zhu, and Chengbu Liu. "Theoretical investigation of gold-catalyzed oxidative Csp3–Csp2 bond formation via aromatic C–H activation." RSC Advances 5, no. 97 (2015): 80048–56. http://dx.doi.org/10.1039/c5ra16359e.
Повний текст джерелаSong, Liangliang, Guilong Tian, Johan Van der Eycken, and Erik V. Van der Eycken. "Intramolecular cascade annulation triggered by rhodium(III)-catalyzed sequential C(sp2)–H activation and C(sp3)–H amination." Beilstein Journal of Organic Chemistry 15 (February 27, 2019): 571–76. http://dx.doi.org/10.3762/bjoc.15.52.
Повний текст джерелаMoghimi, Setareh, Mohammad Mahdavi, Abbas Shafiee, and Alireza Foroumadi. "Transition-Metal-Catalyzed Acyloxylation: Activation of C(sp2)-H and C(sp3)-H Bonds." European Journal of Organic Chemistry 2016, no. 20 (June 19, 2016): 3282–99. http://dx.doi.org/10.1002/ejoc.201600138.
Повний текст джерелаDhara, Shubhendu, Raju Singha, Atiur Ahmed, Haridas Mandal, Munmun Ghosh, Yasin Nuree та Jayanta K. Ray. "Synthesis of α, β and γ-carbolines via Pd-mediated Csp2-H/N–H activation". RSC Adv. 4, № 85 (2014): 45163–67. http://dx.doi.org/10.1039/c4ra08457h.
Повний текст джерелаShin, Seohyun, Dongjin Kang, Woo Hyung Jeon, and Phil Ho Lee. "Synthesis of ethoxy dibenzooxaphosphorin oxides through palladium-catalyzed C(sp2)–H activation/C–O formation." Beilstein Journal of Organic Chemistry 10 (May 23, 2014): 1220–27. http://dx.doi.org/10.3762/bjoc.10.120.
Повний текст джерелаZhang, Hongyu, and Shangdong Yang. "Palladium-catalyzed R2(O)P-directed C(sp2)-H activation." Science China Chemistry 58, no. 8 (April 15, 2015): 1280–85. http://dx.doi.org/10.1007/s11426-015-5382-1.
Повний текст джерелаSahoo, Sumeet Ranjan, Subhabrata Dutta, Shaeel A. Al-Thabaiti, Mohamed Mokhtar, and Debabrata Maiti. "Transition metal catalyzed C–H bond activation by exo-metallacycle intermediates." Chemical Communications 57, no. 90 (2021): 11885–903. http://dx.doi.org/10.1039/d1cc05042g.
Повний текст джерелаSun, Qiao, and Naohiko Yoshikai. "Cobalt-catalyzed C(sp2)–H/C(sp3)–H coupling via directed C–H activation and 1,5-hydrogen atom transfer." Organic Chemistry Frontiers 5, no. 4 (2018): 582–85. http://dx.doi.org/10.1039/c7qo00906b.
Повний текст джерелаLi, Guang-Hui, Dao-Qing Dong, Xian-Yong Yu, and Zu-Li Wang. "Direct synthesis of 8-acylated quinoline N-oxidesviapalladium-catalyzed selective C–H activation and C(sp2)–C(sp2) cleavage." New Journal of Chemistry 43, no. 4 (2019): 1667–70. http://dx.doi.org/10.1039/c8nj05374j.
Повний текст джерелаPark, Ji Eun, and Youn K. Kang. "Evidence of a Wheland Intermediate in Carboxylate-Assisted C(sp2)−H Activation by Pd(IV) Active Catalyst Species Studied via DFT Calculations." Catalysts 13, no. 4 (April 11, 2023): 724. http://dx.doi.org/10.3390/catal13040724.
Повний текст джерелаWang, Xiao, Ming-Zhu Lu, and Teck-Peng Loh. "Transition-Metal-Catalyzed C–C Bond Macrocyclization via Intramolecular C–H Bond Activation." Catalysts 13, no. 2 (February 17, 2023): 438. http://dx.doi.org/10.3390/catal13020438.
Повний текст джерелаValentini, Federica, Oriana Piermatti, and Luigi Vaccaro. "Metal and Metal Oxide Nanoparticles Catalyzed C–H Activation for C–O and C–X (X = Halogen, B, P, S, Se) Bond Formation." Catalysts 13, no. 1 (December 22, 2022): 16. http://dx.doi.org/10.3390/catal13010016.
Повний текст джерелаZucca, Antonio, Sergio Stoccoro, Maria Agostina Cinellu, Giovanni Minghetti, and Mario Manassero. "Cyclometallated derivatives of rhodium(III). Activation of C(sp3)–H vs. C(sp2)–H bonds." Journal of the Chemical Society, Dalton Transactions, no. 19 (1999): 3431–37. http://dx.doi.org/10.1039/a903614h.
Повний текст джерелаPrajapati, Ramanand, Ajay Kant Gola, Amrendra Kumar, Shubham Jaiswal, and Narender Tadigoppula. "o-Acetoxylation of oxo-benzoxazines via C–H activation by palladium(ii)/aluminium oxide." New Journal of Chemistry 46, no. 12 (2022): 5719–24. http://dx.doi.org/10.1039/d2nj00134a.
Повний текст джерелаMaraswami, Manikantha, and Teck-Peng Loh. "Transition-Metal-Catalyzed Alkenyl sp2 C–H Activation: A Short Account." Synthesis 51, no. 05 (January 23, 2019): 1049–62. http://dx.doi.org/10.1055/s-0037-1611649.
Повний текст джерелаUttry, Alexander, and Manuel van Gemmeren. "Direct C(sp3)–H Activation of Carboxylic Acids." Synthesis 52, no. 04 (October 17, 2019): 479–88. http://dx.doi.org/10.1055/s-0039-1690720.
Повний текст джерелаBettadapur, Kiran R., Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "A deciduous directing group approach for the addition of aryl and vinyl nucleophiles to maleimides." Chemical Communications 53, no. 46 (2017): 6251–54. http://dx.doi.org/10.1039/c7cc02392h.
Повний текст джерелаLiu, Weidong, Qingzhen Yu, Le'an Hu, Zenghua Chen, and Jianhui Huang. "Modular synthesis of dihydro-isoquinolines: palladium-catalyzed sequential C(sp2)–H and C(sp3)–H bond activation." Chemical Science 6, no. 10 (2015): 5768–72. http://dx.doi.org/10.1039/c5sc01482d.
Повний текст джерелаSeth, Kapileswar, Manesh Nautiyal, Priyank Purohit, Naisargee Parikh, and Asit K. Chakraborti. "Palladium catalyzed Csp2–H activation for direct aryl hydroxylation: the unprecedented role of 1,4-dioxane as a source of hydroxyl radicals." Chemical Communications 51, no. 1 (2015): 191–94. http://dx.doi.org/10.1039/c4cc06864e.
Повний текст джерелаVerma, Ashish Kumar, Ande Chennaiah, Sateesh Dubbu, and Yashwant D. Vankar. "Palladium catalyzed synthesis of sugar-fused indolines via C(sp2)–H/N H activation." Carbohydrate Research 473 (February 2019): 57–65. http://dx.doi.org/10.1016/j.carres.2018.12.015.
Повний текст джерелаKlare, Hendrik F. T. "Catalytic C–H Arylation of Unactivated C–H Bonds by Silylium Ion-Promoted C(sp2)–F Bond Activation." ACS Catalysis 7, no. 10 (September 20, 2017): 6999–7002. http://dx.doi.org/10.1021/acscatal.7b02658.
Повний текст джерелаCheng, Huiling, Yubo Jiang, Jianhua Yang, Fen Zhao, Yaowen Liu, and Fang Luo. "Selective Diacetoxylation of Disubstituted 1,2,3-Triazoles through Palladium-Catalyzed C–H Activation." Synlett 29, no. 10 (April 12, 2018): 1373–78. http://dx.doi.org/10.1055/s-0036-1591564.
Повний текст джерелаLiu, Yunqi, Yudong Yang, Chunxia Wang, Zhishuo Wang, and Jingsong You. "Rhodium(iii)-catalyzed regioselective oxidative annulation of anilines and allylbenzenes via C(sp3)–H/C(sp2)–H bond cleavage." Chemical Communications 55, no. 8 (2019): 1068–71. http://dx.doi.org/10.1039/c8cc09099h.
Повний текст джерелаZhang, Yanghui, and Bin Wan. "Synthesis of Unsymmetrically Substituted Tetraphenylenes through Palladium-Catalyzed C(sp2)–H Activation." Synthesis 53, no. 18 (March 8, 2021): 3299–306. http://dx.doi.org/10.1055/a-1416-9737.
Повний текст джерелаCurto, John M., and Marisa C. Kozlowski. "Chemoselective Activation of sp3 vs sp2 C–H Bonds with Pd(II)." Journal of the American Chemical Society 137, no. 1 (December 29, 2014): 18–21. http://dx.doi.org/10.1021/ja5093166.
Повний текст джерелаLi, Bin, and Pierre H. Dixneuf. "sp2 C–H bond activation in water and catalytic cross-coupling reactions." Chemical Society Reviews 42, no. 13 (2013): 5744. http://dx.doi.org/10.1039/c3cs60020c.
Повний текст джерелаSong, Juan, Yali Li, Wei Sun, Chenglong Yi, Hao Wu, Haotian Wang, Keran Ding, Kang Xiao, and Chao Liu. "Efficient palladium-catalyzed C(sp2)–H activation towards the synthesis of fluorenes." New Journal of Chemistry 40, no. 11 (2016): 9030–33. http://dx.doi.org/10.1039/c6nj02033j.
Повний текст джерелаDai, Hui-Xiong, Ming Shang, Shang-Zheng Sun, Hong-Li Wang, and Ming-Ming Wang. "Recent Progress on Copper-Mediated Directing-Group-Assisted C(sp2)–H Activation." Synthesis 48, no. 24 (September 9, 2016): 4381–99. http://dx.doi.org/10.1055/s-0035-1562795.
Повний текст джерелаKathiravan, Subban, and Ian A. Nicholls. "Cobalt Catalyzed, Regioselective C(sp2)–H Activation of Amides with 1,3-Diynes." Organic Letters 19, no. 18 (August 28, 2017): 4758–61. http://dx.doi.org/10.1021/acs.orglett.7b02119.
Повний текст джерелаGu, Zheng-Yang, Cheng-Guo Liu, Shun-Yi Wang, and Shun-Jun Ji. "Cobalt-Catalyzed Annulation of Amides with Isocyanides via C(sp2)–H Activation." Journal of Organic Chemistry 82, no. 4 (February 8, 2017): 2223–30. http://dx.doi.org/10.1021/acs.joc.6b02797.
Повний текст джерелаTian, Qingshan, Xianmin Chen, Wei Liu, Zechao Wang, Suping Shi, and Chunxiang Kuang. "Regioselective halogenation of 2-substituted-1,2,3-triazoles via sp2 C–H activation." Organic & Biomolecular Chemistry 11, no. 45 (2013): 7830. http://dx.doi.org/10.1039/c3ob41558a.
Повний текст джерелаWang, Yong, and Qiang Zhu. "Palladium(II)-Catalyzed Cycloamidination via C(sp2)H Activation and Isocyanide Insertion." Advanced Synthesis & Catalysis 354, no. 10 (June 29, 2012): 1902–8. http://dx.doi.org/10.1002/adsc.201200106.
Повний текст джерелаTang, Ren-Jin, Cui-Ping Luo, Luo Yang, and Chao-Jun Li. "Rhodium(III)-Catalyzed C(sp2)H Activation and Electrophilic Amidation withN-Fluorobenzenesulfonimide." Advanced Synthesis & Catalysis 355, no. 5 (February 22, 2013): 869–73. http://dx.doi.org/10.1002/adsc.201201133.
Повний текст джерелаCizikovs, Aleksandrs, and Liene Grigorjeva. "Co(III) Intermediates in Cobalt-Catalyzed, Bidentate Chelation Assisted C(sp2)-H Functionalizations." Inorganics 11, no. 5 (April 29, 2023): 194. http://dx.doi.org/10.3390/inorganics11050194.
Повний текст джерелаPashazadeh, Rahim, Saideh Rajai-Daryasarei, Siyavash Mirzaei, Mehdi Soheilizad, Samira Ansari, and Meisam Shabanian. "A Regioselective Approach to C3-Aroylcoumarins via Cobalt-Catalyzed C(sp2)–H Activation Carbonylation of Coumarins." Synthesis 51, no. 15 (April 2, 2019): 3014–20. http://dx.doi.org/10.1055/s-0037-1610702.
Повний текст джерелаSwamy, V. S. V. S. N., Nasrina Parvin, K. Vipin Raj, Kumar Vanka, and Sakya S. Sen. "C(sp3)–F, C(sp2)–F and C(sp3)–H bond activation at silicon(ii) centers." Chemical Communications 53, no. 71 (2017): 9850–53. http://dx.doi.org/10.1039/c7cc05145j.
Повний текст джерелаFujihara, Tetsuaki, Yutaka Tanji, and Yasushi Tsuji. "Palladium-Catalyzed Synthesis of Fluorenes by Intramolecular C(sp2)–H Activation at Room Temperature." Synlett 31, no. 08 (February 4, 2020): 805–8. http://dx.doi.org/10.1055/s-0039-1690812.
Повний текст джерелаKonwar, Manashjyoti, Roktopol Hazarika, and Diganta Sarma. "Synthetic advances in C(sp2)-H/N–H arylation of pyrazole derivatives through activation/substitution." Tetrahedron 102 (December 2021): 132504. http://dx.doi.org/10.1016/j.tet.2021.132504.
Повний текст джерелаYoung, Michael, Mohit Kapoor, Pratibha Chand-Thakuri, Justin Maxwell, Daniel Liu, and Hanyang Zhou. "Carbon Dioxide-Driven Palladium-Catalyzed C–H Activation of Amines: A Unified Approach for the Arylation of Aliphatic and Aromatic Primary and Secondary Amines." Synlett 30, no. 05 (January 8, 2019): 519–24. http://dx.doi.org/10.1055/s-0037-1611381.
Повний текст джерелаZhou, Wei, Hongji Li та Lei Wang. "Direct Carbo-Acylation Reactions of 2-Arylpyridines with α-Diketones via Pd-Catalyzed C–H Activation and Selective C(sp2)–C(sp2) Cleavage". Organic Letters 14, № 17 (27 серпня 2012): 4594–97. http://dx.doi.org/10.1021/ol3020557.
Повний текст джерелаKim, Daeun, Geunho Choi, Weonjeong Kim, Dongwook Kim, Youn K. Kang, and Soon Hyeok Hong. "The site-selectivity and mechanism of Pd-catalyzed C(sp2)–H arylation of simple arenes." Chemical Science 12, no. 1 (2021): 363–73. http://dx.doi.org/10.1039/d0sc05414c.
Повний текст джерелаLi, Dan-Dan, Yi-Xuan Cao, and Guan-Wu Wang. "Palladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp2 C–H bond activation." Organic & Biomolecular Chemistry 13, no. 25 (2015): 6958–64. http://dx.doi.org/10.1039/c5ob00691k.
Повний текст джерелаArevalo, Rebeca, Tyler P. Pabst, and Paul J. Chirik. "C(sp2)–H Borylation of Heterocycles by Well-Defined Bis(silylene)pyridine Cobalt(III) Precatalysts: Pincer Modification, C(sp2)–H Activation, and Catalytically Relevant Intermediates." Organometallics 39, no. 14 (July 8, 2020): 2763–73. http://dx.doi.org/10.1021/acs.organomet.0c00382.
Повний текст джерелаHu, Zhe-Yao, Yan Zhang, Xin-Chang Li, Jing Zi, and Xun-Xiang Guo. "Pd-Catalyzed Intramolecular Chemoselective C(sp2)–H and C(sp3)–H Activation of N-Alkyl-N-arylanthranilic Acids." Organic Letters 21, no. 4 (January 29, 2019): 989–92. http://dx.doi.org/10.1021/acs.orglett.8b03976.
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