Artykuły w czasopismach na temat „C(sp2)-H bond activation”
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Wang, Xiao, Ming-Zhu Lu i Teck-Peng Loh. "Transition-Metal-Catalyzed C–C Bond Macrocyclization via Intramolecular C–H Bond Activation". Catalysts 13, nr 2 (17.02.2023): 438. http://dx.doi.org/10.3390/catal13020438.
Pełny tekst źródłaValentini, Federica, Oriana Piermatti i 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, nr 1 (22.12.2022): 16. http://dx.doi.org/10.3390/catal13010016.
Pełny tekst źródłaPaira, Moumita. "Recent Developments of Palladium-Catalyzed C(sp3)/C(sp2)-H Bond Functionalizations Assisted by 8-Aminoquinoline Bidentate Directing Group". Asian Journal of Chemistry 34, nr 8 (2022): 1958–74. http://dx.doi.org/10.14233/ajchem.2022.23774.
Pełny tekst źródłaLiu, Jialin, Xiaoyu Xiong, Jie Chen, Yuntao Wang, Ranran Zhu i Jianhui Huang. "Double C–H Activation for the C–C bond Formation Reactions". Current Organic Synthesis 15, nr 7 (16.10.2018): 882–903. http://dx.doi.org/10.2174/1570179415666180720111422.
Pełny tekst źródłaCheng, Huiling, Yubo Jiang, Jianhua Yang, Fen Zhao, Yaowen Liu i Fang Luo. "Selective Diacetoxylation of Disubstituted 1,2,3-Triazoles through Palladium-Catalyzed C–H Activation". Synlett 29, nr 10 (12.04.2018): 1373–78. http://dx.doi.org/10.1055/s-0036-1591564.
Pełny tekst źródłaShin, Seohyun, Dongjin Kang, Woo Hyung Jeon i Phil Ho Lee. "Synthesis of ethoxy dibenzooxaphosphorin oxides through palladium-catalyzed C(sp2)–H activation/C–O formation". Beilstein Journal of Organic Chemistry 10 (23.05.2014): 1220–27. http://dx.doi.org/10.3762/bjoc.10.120.
Pełny tekst źródłaLiu, Weidong, Qingzhen Yu, Le'an Hu, Zenghua Chen i Jianhui Huang. "Modular synthesis of dihydro-isoquinolines: palladium-catalyzed sequential C(sp2)–H and C(sp3)–H bond activation". Chemical Science 6, nr 10 (2015): 5768–72. http://dx.doi.org/10.1039/c5sc01482d.
Pełny tekst źródłaBritton, Luke, Jamie H. Docherty, Andrew P. Dominey i Stephen P. Thomas. "Iron-Catalysed C(sp2)-H Borylation Enabled by Carboxylate Activation". Molecules 25, nr 4 (18.02.2020): 905. http://dx.doi.org/10.3390/molecules25040905.
Pełny tekst źródłaGeng, Cuihuan, Sujuan Zhang, Chonggang Duan, Tongxiang Lu, Rongxiu Zhu i Chengbu Liu. "Theoretical investigation of gold-catalyzed oxidative Csp3–Csp2 bond formation via aromatic C–H activation". RSC Advances 5, nr 97 (2015): 80048–56. http://dx.doi.org/10.1039/c5ra16359e.
Pełny tekst źródłaLi, Guang-Hui, Dao-Qing Dong, Xian-Yong Yu i 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, nr 4 (2019): 1667–70. http://dx.doi.org/10.1039/c8nj05374j.
Pełny tekst źródłaKlare, Hendrik F. T. "Catalytic C–H Arylation of Unactivated C–H Bonds by Silylium Ion-Promoted C(sp2)–F Bond Activation". ACS Catalysis 7, nr 10 (20.09.2017): 6999–7002. http://dx.doi.org/10.1021/acscatal.7b02658.
Pełny tekst źródłaSahoo, Sumeet Ranjan, Subhabrata Dutta, Shaeel A. Al-Thabaiti, Mohamed Mokhtar i Debabrata Maiti. "Transition metal catalyzed C–H bond activation by exo-metallacycle intermediates". Chemical Communications 57, nr 90 (2021): 11885–903. http://dx.doi.org/10.1039/d1cc05042g.
Pełny tekst źródłaCizikovs, Aleksandrs, i Liene Grigorjeva. "Co(III) Intermediates in Cobalt-Catalyzed, Bidentate Chelation Assisted C(sp2)-H Functionalizations". Inorganics 11, nr 5 (29.04.2023): 194. http://dx.doi.org/10.3390/inorganics11050194.
Pełny tekst źródłaPashazadeh, Rahim, Saideh Rajai-Daryasarei, Siyavash Mirzaei, Mehdi Soheilizad, Samira Ansari i Meisam Shabanian. "A Regioselective Approach to C3-Aroylcoumarins via Cobalt-Catalyzed C(sp2)–H Activation Carbonylation of Coumarins". Synthesis 51, nr 15 (2.04.2019): 3014–20. http://dx.doi.org/10.1055/s-0037-1610702.
Pełny tekst źródłaAbdelmalek, Fatiha, Fazia Derridj, Safia Djebbar, Jean-François Soulé i Henri Doucet. "Efficient synthesis of π-conjugated molecules incorporating fluorinated phenylene units through palladium-catalyzed iterative C(sp2)–H bond arylations". Beilstein Journal of Organic Chemistry 11 (28.10.2015): 2012–20. http://dx.doi.org/10.3762/bjoc.11.218.
Pełny tekst źródłaBettadapur, Kiran R., Veeranjaneyulu Lanke i Kandikere Ramaiah Prabhu. "A deciduous directing group approach for the addition of aryl and vinyl nucleophiles to maleimides". Chemical Communications 53, nr 46 (2017): 6251–54. http://dx.doi.org/10.1039/c7cc02392h.
Pełny tekst źródłaXu, Runsheng, Yueer Zhu, Feixiang Xiong i Suli Tong. "Direct Sulfoxidation of Aromatic Methyl Thioethers with Aryl Halides by Copper-Catalyzed C(sp3)–H Bond Activation". Catalysts 9, nr 1 (21.01.2019): 105. http://dx.doi.org/10.3390/catal9010105.
Pełny tekst źródłaLi, Bin, i Pierre H. Dixneuf. "sp2 C–H bond activation in water and catalytic cross-coupling reactions". Chemical Society Reviews 42, nr 13 (2013): 5744. http://dx.doi.org/10.1039/c3cs60020c.
Pełny tekst źródłaSwamy, V. S. V. S. N., Nasrina Parvin, K. Vipin Raj, Kumar Vanka i Sakya S. Sen. "C(sp3)–F, C(sp2)–F and C(sp3)–H bond activation at silicon(ii) centers". Chemical Communications 53, nr 71 (2017): 9850–53. http://dx.doi.org/10.1039/c7cc05145j.
Pełny tekst źródłaYamaoka, Yousuke, i Hideto Miyabe. "NHC-Catalyzed Reaction of Aldehydes for C(sp2)–O Bond Formation". Catalysts 14, nr 4 (22.03.2024): 219. http://dx.doi.org/10.3390/catal14040219.
Pełny tekst źródłaDutta, Uttam, Sudip Maiti, Trisha Bhattacharya i Debabrata Maiti. "Arene diversification through distal C(sp2)−H functionalization". Science 372, nr 6543 (13.05.2021): eabd5992. http://dx.doi.org/10.1126/science.abd5992.
Pełny tekst źródłaCui, Bingcun, Guosheng Huang, Jin Liu, Shaofen Jin, Yingxing Zhou, Dongmei Ni, Tingting Liu, Gang Hu i Xin Yu. "Palladium-Catalyzed ortho-Monoacylation of Arenes with Aldehydes via 1,2,4-Benzotriazine-Directed C–H Bond Activation". Synthesis 52, nr 09 (10.02.2020): 1407–16. http://dx.doi.org/10.1055/s-0039-1691564.
Pełny tekst źródłaLiu, Yunqi, Yudong Yang, Chunxia Wang, Zhishuo Wang i Jingsong You. "Rhodium(iii)-catalyzed regioselective oxidative annulation of anilines and allylbenzenes via C(sp3)–H/C(sp2)–H bond cleavage". Chemical Communications 55, nr 8 (2019): 1068–71. http://dx.doi.org/10.1039/c8cc09099h.
Pełny tekst źródłaUttry, Alexander, i Manuel van Gemmeren. "Direct C(sp3)–H Activation of Carboxylic Acids". Synthesis 52, nr 04 (17.10.2019): 479–88. http://dx.doi.org/10.1055/s-0039-1690720.
Pełny tekst źródłaYoung, Michael, Mohit Kapoor, Pratibha Chand-Thakuri, Justin Maxwell, Daniel Liu i 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, nr 05 (8.01.2019): 519–24. http://dx.doi.org/10.1055/s-0037-1611381.
Pełny tekst źródłaSharma, Satyasheel, Neeraj Kumar Mishra, Youngmi Shin i In Su Kim. "Transition-Metal-Catalyzed Oxidative and Decarboxylative Acylations through sp2 C-H Bond Activation". Current Organic Chemistry 20, nr 5 (3.12.2015): 471–511. http://dx.doi.org/10.2174/1385272819666150122234834.
Pełny tekst źródłaLi, Dan-Dan, Yi-Xuan Cao i Guan-Wu Wang. "Palladium-catalyzed ortho-acyloxylation of N-nitrosoanilines via direct sp2 C–H bond activation". Organic & Biomolecular Chemistry 13, nr 25 (2015): 6958–64. http://dx.doi.org/10.1039/c5ob00691k.
Pełny tekst źródłaZhang, Zhiguo, Jingjing Qian, Guisheng Zhang, Nana Ma, Qingfeng Liu, Tongxin Liu, Kai Sun i Lei Shi. "Copper(i) catalyzed C(sp2)–N bond formation: synthesis of pyrrolo[3,2-c]quinolinone derivatives". Organic Chemistry Frontiers 3, nr 3 (2016): 344–48. http://dx.doi.org/10.1039/c5qo00417a.
Pełny tekst źródłaMaraswami, Manikantha, i Teck-Peng Loh. "Transition-Metal-Catalyzed Alkenyl sp2 C–H Activation: A Short Account". Synthesis 51, nr 05 (23.01.2019): 1049–62. http://dx.doi.org/10.1055/s-0037-1611649.
Pełny tekst źródłaMao, Jiangang, i Weiliang Bao. "Palladium-catalyzed [2+1+1] annulation of norbornenes with (z)-bromostyrenes: synthesis of bismethylenecyclobutanes via twofold C(sp2)–H bond activation". Chem. Commun. 50, nr 99 (2014): 15726–29. http://dx.doi.org/10.1039/c4cc06545j.
Pełny tekst źródłaMoghimi, Setareh, Mohammad Mahdavi, Abbas Shafiee i Alireza Foroumadi. "Transition-Metal-Catalyzed Acyloxylation: Activation of C(sp2)-H and C(sp3)-H Bonds". European Journal of Organic Chemistry 2016, nr 20 (19.06.2016): 3282–99. http://dx.doi.org/10.1002/ejoc.201600138.
Pełny tekst źródłaYuan, Yizhi, Song Song i Ning Jiao. "Recent Development in Pd-Catalyzedmeta-C(sp2)-H Bond Activation Based on Directing Strategy". Acta Chimica Sinica 73, nr 12 (2015): 1231. http://dx.doi.org/10.6023/a15050319.
Pełny tekst źródłaNan, Jiang, Zhijun Zuo, Lei Luo, Lu Bai, Huayu Zheng, Yini Yuan, Jingjing Liu, Xinjun Luan i Yaoyu Wang. "RuII-Catalyzed Vinylative Dearomatization of Naphthols via a C(sp2)–H Bond Activation Approach". Journal of the American Chemical Society 135, nr 46 (6.11.2013): 17306–9. http://dx.doi.org/10.1021/ja410060e.
Pełny tekst źródłaDhara, Shubhendu, Raju Singha, Atiur Ahmed, Haridas Mandal, Munmun Ghosh, Yasin Nuree i Jayanta K. Ray. "Synthesis of α, β and γ-carbolines via Pd-mediated Csp2-H/N–H activation". RSC Adv. 4, nr 85 (2014): 45163–67. http://dx.doi.org/10.1039/c4ra08457h.
Pełny tekst źródłaNaveen, Kanagaraj, Avanashiappan Nandakumar i Paramasivan Perumal. "Synthesis of 4-Alkylidene-Substituted 1,2,3,4-Tetrahydroisoquinolines via Palladium-Catalyzed Carbopalladation/C–H Activation of 2-Bromobenzyl-N-propargylamines". Synthesis 47, nr 11 (18.03.2015): 1633–42. http://dx.doi.org/10.1055/s-0034-1380414.
Pełny tekst źródłaLin, Yumei, Hui Xu, Lei Gong, Ting Bin Wen, Xu-Min He i Haiping Xia. "C−H Bond Activation and Subsequent C(sp2)−C(sp3) Bond Formation: Coupling of Bromomethyl and Triphenylphosphine in an Iridium Complex". Organometallics 29, nr 13 (12.07.2010): 2904–10. http://dx.doi.org/10.1021/om100187t.
Pełny tekst źródłaZucca, Antonio, Sergio Stoccoro, Maria Agostina Cinellu, Giovanni Minghetti i Mario Manassero. "Cyclometallated derivatives of rhodium(III). Activation of C(sp3)–H vs. C(sp2)–H bonds". Journal of the Chemical Society, Dalton Transactions, nr 19 (1999): 3431–37. http://dx.doi.org/10.1039/a903614h.
Pełny tekst źródłaPrajapati, Ramanand, Ajay Kant Gola, Amrendra Kumar, Shubham Jaiswal i Narender Tadigoppula. "o-Acetoxylation of oxo-benzoxazines via C–H activation by palladium(ii)/aluminium oxide". New Journal of Chemistry 46, nr 12 (2022): 5719–24. http://dx.doi.org/10.1039/d2nj00134a.
Pełny tekst źródłaMondal, Biplab, i Brindaban Roy. "Di-tert-butyl peroxide (DTBP) promoted dehydrogenative coupling: an expedient and metal-free synthesis of oxindoles via intramolecular C(sp2)–H and C(sp3)–H bond activation". RSC Advances 5, nr 85 (2015): 69119–23. http://dx.doi.org/10.1039/c5ra09055e.
Pełny tekst źródłaShi, Yun, Meng-Sheng Li, Fangdong Zhang i Baohua Chen. "Nickel(ii)-catalyzed tandem C(sp2)–H bond activation and annulation of arenes with gem-dibromoalkenes". RSC Advances 8, nr 50 (2018): 28668–75. http://dx.doi.org/10.1039/c8ra03278e.
Pełny tekst źródłaZhang, Chun, Jing Ji i Peipei Sun. "Palladium-Catalyzed Alkenylation via sp2 C–H Bond Activation Using Phenolic Hydroxyl as the Directing Group". Journal of Organic Chemistry 79, nr 7 (20.03.2014): 3200–3205. http://dx.doi.org/10.1021/jo4028825.
Pełny tekst źródłaNan, Jiang, Zhijun Zuo, Lei Luo, Lu Bai, Huayu Zheng, Yini Yuan, Jingjing Liu, Xinjun Luan i Yaoyu Wang. "ChemInform Abstract: RuII-Catalyzed Vinylative Dearomatization of Naphthols via a C(sp2)-H Bond Activation Approach." ChemInform 45, nr 23 (22.05.2014): no. http://dx.doi.org/10.1002/chin.201423075.
Pełny tekst źródłaShen, Guodong, Lingyu Zhao, Yichen Wang, Wenfang Xia, Mingsen Yang i Tongxin Zhang. "Palladium–copper catalyzed C(sp3)–C(sp2) bond C–H activation cross-coupling reaction: selective arylation to synthesize 9-aryl-9H-xanthene and 9,9-diaryl-xanthene derivatives". RSC Advances 6, nr 88 (2016): 84748–51. http://dx.doi.org/10.1039/c6ra17546e.
Pełny tekst źródłaMonsigny, Louis, Floriane Doche i Tatiana Besset. "Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview". Beilstein Journal of Organic Chemistry 19 (17.04.2023): 448–73. http://dx.doi.org/10.3762/bjoc.19.35.
Pełny tekst źródłaCurto, John M., i Marisa C. Kozlowski. "Chemoselective Activation of sp3 vs sp2 C–H Bonds with Pd(II)". Journal of the American Chemical Society 137, nr 1 (29.12.2014): 18–21. http://dx.doi.org/10.1021/ja5093166.
Pełny tekst źródłaCarr, Kevin J. T., David L. Davies, Stuart A. Macgregor, Kuldip Singh i Barbara Villa-Marcos. "Metal control of selectivity in acetate-assisted C–H bond activation: an experimental and computational study of heterocyclic, vinylic and phenylic C(sp2)–H bonds at Ir and Rh". Chem. Sci. 5, nr 6 (2014): 2340–46. http://dx.doi.org/10.1039/c4sc00738g.
Pełny tekst źródłaYadav, Lalit, Mohit K. Tiwari, Bharti Rajesh Kumar Shyamlal i Sandeep Chaudhary. "Organocatalyst in Direct C(sp2)–H Arylation of Unactivated Arenes: [1-(2-Hydroxyethyl)-piperazine]-Catalyzed Inter-/Intra-molecular C–H Bond Activation". Journal of Organic Chemistry 85, nr 12 (22.05.2020): 8121–41. http://dx.doi.org/10.1021/acs.joc.0c01019.
Pełny tekst źródłaDing, Jun, Ying Guo, Ling-Yan Shao, Fei-Yi Zhao, Dao-Hua Liao, Hong-Wei Liu i Ya-Fei Ji. "Palladium-catalyzed multi-acetoxylation of 1,3-disubstituted 1H-pyrazole-5-carboxylates via direct C(sp2)H or C(sp3)H bond activation". Chinese Chemical Letters 27, nr 10 (październik 2016): 1617–21. http://dx.doi.org/10.1016/j.cclet.2016.04.007.
Pełny tekst źródłaEom, Dahan, Yeonseok Jeong, Yea Rin Kim, Euichul Lee, Wonseok Choi i Phil Ho Lee. "Palladium-Catalyzed C(sp2 and sp3)–H Activation/C–O Bond Formation: Synthesis of Benzoxaphosphole 1- and 2-Oxides". Organic Letters 15, nr 20 (8.10.2013): 5210–13. http://dx.doi.org/10.1021/ol402736v.
Pełny tekst źródłaBunescu, Ala, Tiffany Piou, Qian Wang i Jieping Zhu. "Pd-Catalyzed Dehydrogenative Aryl–Aryl Bond Formation via Double C(sp2)–H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles". Organic Letters 17, nr 2 (19.12.2014): 334–37. http://dx.doi.org/10.1021/ol503442n.
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