Статті в журналах з теми "Au alkynes hydroarylation"
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Duan, Chang-Lin, Xing-Yu Liu, Yun-Xuan Tan, Rui Ding, Shiping Yang, Ping Tian, and Guo-Qiang Lin. "Acetic Acid-Promoted Rhodium(III)-Catalyzed Hydroarylation of Terminal Alkynes." Synlett 30, no. 08 (March 26, 2019): 932–38. http://dx.doi.org/10.1055/s-0037-1611780.
Повний текст джерелаTubaro, Cristina, Marco Baron, Andrea Biffis, and Marino Basato. "Alkyne hydroarylation with Au N-heterocyclic carbene catalysts." Beilstein Journal of Organic Chemistry 9 (February 5, 2013): 246–53. http://dx.doi.org/10.3762/bjoc.9.29.
Повний текст джерелаZhang, Chaofeng, Songkui Lv, Yanru Wang, Jingyi Zhang, Xiao-Na Wang, and Junbiao Chang. "Metal-free intramolecular hydroarylation of alkynes." Organic Chemistry Frontiers 9, no. 5 (2022): 1300–1307. http://dx.doi.org/10.1039/d1qo01831k.
Повний текст джерелаZhao, JiaKai, Qi Mou, RuiHan Niu, RuYuan Zhao, and Bo Sun. "Environmentally Friendly Cp*Co(III)-catalyzed C-H Bond Hydroarylation of Alkynes." Journal of Physics: Conference Series 2076, no. 1 (November 1, 2021): 012038. http://dx.doi.org/10.1088/1742-6596/2076/1/012038.
Повний текст джерелаde Mendoza, Paula, and Antonio M. Echavarren. "Synthesis of arenes and heteroarenes by hydroarylation reactions catalyzed by electrophilic metal complexes." Pure and Applied Chemistry 82, no. 4 (March 10, 2010): 801–20. http://dx.doi.org/10.1351/pac-con-09-10-06.
Повний текст джерелаThowfik, Salam, C. M. A. Afsina, and Gopinathan Anilkumar. "Ruthenium-catalyzed hydroarylation reactions as the strategy towards the synthesis of alkylated arenes and substituted alkenes." RSC Advances 13, no. 9 (2023): 6246–63. http://dx.doi.org/10.1039/d3ra00211j.
Повний текст джерелаPanda, Niranjan, Irshad Mattan, Subhadra Ojha, and Chandra Shekhar Purohit. "Synthesis of medium-sized (6–7–6) ring compounds by iron-catalyzed dehydrogenative C–H activation/annulation." Organic & Biomolecular Chemistry 16, no. 42 (2018): 7861–70. http://dx.doi.org/10.1039/c8ob01496e.
Повний текст джерелаLuo, Cuicui, Hongwei Yang, Rongfang Mao, Chunxu Lu, and Guangbin Cheng. "An efficient Au(i) catalyst for double hydroarylation of alkynes with heteroarenes." New Journal of Chemistry 39, no. 5 (2015): 3417–23. http://dx.doi.org/10.1039/c4nj02170c.
Повний текст джерелаYamamoto, Y., E. Ohkubo, and M. Shibuya. "Selective synthesis of trisubstituted (trifluoromethyl)alkenes via ligand-free Cu-catalyzed syn hydroarylation, hydroalkenylation and hydroallylation of (trifluoromethyl)alkynes." Green Chemistry 18, no. 17 (2016): 4628–32. http://dx.doi.org/10.1039/c6gc01782g.
Повний текст джерелаChen, Bin, Yan Jiang, Jiang Cheng, and Jin-Tao Yu. "Rhodium-catalyzed hydroarylation of alkynes via tetrazole-directed C–H activation." Organic & Biomolecular Chemistry 13, no. 10 (2015): 2901–4. http://dx.doi.org/10.1039/c5ob00064e.
Повний текст джерелаReetz, Manfred T., and Knut Sommer. "Gold-Catalyzed Hydroarylation of Alkynes." European Journal of Organic Chemistry 2003, no. 18 (September 2003): 3485–96. http://dx.doi.org/10.1002/ejoc.200300260.
Повний текст джерелаLaFortune, James H. W., Julia M. Bayne, Timothy C. Johnstone, Louie Fan, and Douglas W. Stephan. "Catalytic double hydroarylation of alkynes to 9,9-disubstituted 9,10-dihydroacridine derivatives by an electrophilic phenoxyphosphonium dication." Chemical Communications 53, no. 100 (2017): 13312–15. http://dx.doi.org/10.1039/c7cc08037a.
Повний текст джерелаPadala, Kishor, and Masilamani Jeganmohan. "Ruthenium-catalyzed highly regio- and stereoselective hydroarylation of aromatic sulfoxides with alkynes via C–H bond activation." Chem. Commun. 50, no. 93 (2014): 14573–76. http://dx.doi.org/10.1039/c4cc06426g.
Повний текст джерелаTakahashi, Ikko, Takeshi Fujita, Noriaki Shoji, and Junji Ichikawa. "Brønsted acid-catalysed hydroarylation of unactivated alkynes in a fluoroalcohol–hydrocarbon biphasic system: construction of phenanthrene frameworks." Chemical Communications 55, no. 63 (2019): 9267–70. http://dx.doi.org/10.1039/c9cc04152d.
Повний текст джерелаHu, Feng, and Michal Szostak. "Ruthenium(0)-catalyzed hydroarylation of alkynes via ketone-directed C–H functionalization using in situ-generated ruthenium complexes." Chemical Communications 52, no. 62 (2016): 9715–18. http://dx.doi.org/10.1039/c6cc04537e.
Повний текст джерелаEchavarren, Antonio M., and Cristina Nevado. "Transition Metal-Catalyzed Hydroarylation of Alkynes." Synthesis 2005, no. 02 (2005): 167–82. http://dx.doi.org/10.1055/s-2005-861781.
Повний текст джерелаCampagne, Jean-Marc, Christophe Dal Zotto, Johny Wehbe, and David Virieux. "FeCl3-Catalyzed Intramolecular Hydroarylation of Alkynes." Synlett 2008, no. 13 (July 15, 2008): 2033–35. http://dx.doi.org/10.1055/s-2008-1077954.
Повний текст джерелаWang, Yun-Long, Wen-Man Zhang, Jian-Jun Dai, Yi-Si Feng, and Hua-Jian Xu. "Cu-catalyzed intramolecular hydroarylation of alkynes." RSC Adv. 4, no. 106 (November 11, 2014): 61706–10. http://dx.doi.org/10.1039/c4ra12258e.
Повний текст джерелаNakao, Yoshiaki. "Hydroarylation of alkynes catalyzed by nickel." Chemical Record 11, no. 5 (September 6, 2011): 242–51. http://dx.doi.org/10.1002/tcr.201100023.
Повний текст джерелаde Mendoza, Paula, and Antonio M. Echavarren. "ChemInform Abstract: Intramolecular Hydroarylation of Alkynes." ChemInform 44, no. 1 (January 1, 2013): no. http://dx.doi.org/10.1002/chin.201301177.
Повний текст джерелаManikandan, Rajendran, and Masilamani Jeganmohan. "Recent advances in the ruthenium-catalyzed hydroarylation of alkynes with aromatics: synthesis of trisubstituted alkenes." Organic & Biomolecular Chemistry 13, no. 42 (2015): 10420–36. http://dx.doi.org/10.1039/c5ob01472g.
Повний текст джерелаQian, Zhen-Chao, Jun Zhou, Bo Li, Fang Hu, and Bing-Feng Shi. "Rh(iii)-catalyzed regioselective hydroarylation of alkynes via directed C–H functionalization of pyridines." Org. Biomol. Chem. 12, no. 22 (2014): 3594–97. http://dx.doi.org/10.1039/c4ob00612g.
Повний текст джерелаShibuya, Tetsuro, Kyosuke Nakamura, and Ken Tanaka. "Cationic gold(I) axially chiral biaryl bisphosphine complex-catalyzed atropselective synthesis of heterobiaryls." Beilstein Journal of Organic Chemistry 7 (July 6, 2011): 944–50. http://dx.doi.org/10.3762/bjoc.7.105.
Повний текст джерелаGu, Guangxin, Hao Guo, Yang Li, Yu Wang, Dawen Xu, and Ruiwen Jin. "AlCl3-Catalyzed Intramolecular Hydroarylation of Arenes with Alkynes." Synlett 28, no. 16 (July 6, 2017): 2159–62. http://dx.doi.org/10.1055/s-0036-1588479.
Повний текст джерелаXie, Jin, Zhongfei Yan, and Chengjian Zhu. "Manganese(I)-Catalyzed Selective Functionalization of Alkynes." Synlett 30, no. 02 (November 30, 2018): 124–28. http://dx.doi.org/10.1055/s-0037-1610335.
Повний текст джерелаSchipper, Derek J., Marieke Hutchinson, and Keith Fagnou. "Rhodium(III)-Catalyzed Intermolecular Hydroarylation of Alkynes." Journal of the American Chemical Society 132, no. 20 (May 26, 2010): 6910–11. http://dx.doi.org/10.1021/ja103080d.
Повний текст джерелаXu, Dawen, Ramon Rios, Feifei Ba, Dongmei Ma, Guangxin Gu, Aishun Ding, Yunyan Kuang, and Hao Guo. "Photoinduced Intramolecular Haloarylation and Hydroarylation of Alkynes." Asian Journal of Organic Chemistry 5, no. 8 (June 17, 2016): 981–85. http://dx.doi.org/10.1002/ajoc.201600232.
Повний текст джерелаGodoi, Marla N., Francisco de Azambuja, Pablo David G. Martinez, Nelson H. Morgon, Vanessa G. Santos, Thaís Regiani, Denis Lesage, et al. "Revisiting the Intermolecular Fujiwara Hydroarylation of Alkynes." European Journal of Organic Chemistry 2017, no. 13 (April 3, 2017): 1794–803. http://dx.doi.org/10.1002/ejoc.201700033.
Повний текст джерелаGuo, Jing, Odelia Cheong, Karlee L. Bamford, Jiliang Zhou, and Douglas W. Stephan. "Frustrated Lewis pair-catalyzed double hydroarylation of alkynes with N-substituted pyrroles." Chemical Communications 56, no. 12 (2020): 1855–58. http://dx.doi.org/10.1039/c9cc08654d.
Повний текст джерелаFujiwara, Yuzo, and Chengguo Jia. "New developments in transition metal-catalyzed synthetic reactions via C-H bond activation." Pure and Applied Chemistry 73, no. 2 (January 1, 2001): 319–24. http://dx.doi.org/10.1351/pac200173020319.
Повний текст джерелаPascual, Sergio, Christophe Bour, Paula de Mendoza, and Antonio M. Echavarren. "Synthesis of fluoranthenes by hydroarylation of alkynes catalyzed by gold(I) or gallium trichloride." Beilstein Journal of Organic Chemistry 7 (November 14, 2011): 1520–25. http://dx.doi.org/10.3762/bjoc.7.178.
Повний текст джерелаCacchi, Sandro, Giancarlo Fabrizi, Antonella Goggiamani, and Daniela Persiani. "Palladium-Catalyzed Hydroarylation of Alkynes with Arenediazonium Salts." Organic Letters 10, no. 8 (April 2008): 1597–600. http://dx.doi.org/10.1021/ol800266e.
Повний текст джерелаXu, Xiaoling, Jiuxi Chen, Wenxia Gao, Huayue Wu, Jinchang Ding, and Weike Su. "Palladium-catalyzed hydroarylation of alkynes with arylboronic acids." Tetrahedron 66, no. 13 (March 2010): 2433–38. http://dx.doi.org/10.1016/j.tet.2010.01.086.
Повний текст джерелаZhang, Jing, Ruja Shrestha, John F. Hartwig, and Pinjing Zhao. "A decarboxylative approach for regioselective hydroarylation of alkynes." Nature Chemistry 8, no. 12 (September 5, 2016): 1144–51. http://dx.doi.org/10.1038/nchem.2602.
Повний текст джерелаNakao, Yoshiaki. "ChemInform Abstract: Hydroarylation of Alkynes Catalyzed by Nickel." ChemInform 43, no. 7 (January 23, 2012): no. http://dx.doi.org/10.1002/chin.201207268.
Повний текст джерелаWang, Yun-Long, Wen-Man Zhang, Jian-Jun Dai, Yi-Si Feng, and Hua-Jian Xu. "ChemInform Abstract: Cu-Catalyzed Intramolecular Hydroarylation of Alkynes." ChemInform 46, no. 19 (April 23, 2015): no. http://dx.doi.org/10.1002/chin.201519041.
Повний текст джерелаWang, Xulun, Lihong Zhou, and Wenjun Lu. "Hydroarylation of Alkynes via Aryl C-H Bond Cleavage." Current Organic Chemistry 14, no. 3 (February 1, 2010): 289–307. http://dx.doi.org/10.2174/138527210790231964.
Повний текст джерелаHahn, Christine, Mayra Miranda, Nagendra P. B. Chittineni, Trent A. Pinion, and Ricardo Perez. "Mechanistic Studies on Platinum(II) Catalyzed Hydroarylation of Alkynes." Organometallics 33, no. 12 (June 11, 2014): 3040–50. http://dx.doi.org/10.1021/om5003123.
Повний текст джерелаBhaskar, G., C. Saikumar, and P. T. Perumal. "Indium(III) bromide-catalyzed hydroarylation of alkynes with indoles." Tetrahedron Letters 51, no. 23 (June 2010): 3141–45. http://dx.doi.org/10.1016/j.tetlet.2010.04.036.
Повний текст джерелаLiu, Saiwen, Yang Bai, Xiangxiang Cao, Fuhong Xiao, and Guo-Jun Deng. "Palladium-catalyzed desulfitative hydroarylation of alkynes with sodium sulfinates." Chemical Communications 49, no. 68 (2013): 7501. http://dx.doi.org/10.1039/c3cc43723j.
Повний текст джерелаHanna, Luke E., Mikhail O. Konev, and Elizabeth R. Jarvo. "Nickel-Catalyzed Directed Hydroarylation of Alkynes with Boronic Acids." European Journal of Organic Chemistry 2019, no. 1 (November 25, 2018): 184–87. http://dx.doi.org/10.1002/ejoc.201801494.
Повний текст джерелаSchipper, Derek J., Marieke Hutchinson, and Keith Fagnou. "ChemInform Abstract: Rhodium(III)-Catalyzed Intermolecular Hydroarylation of Alkynes." ChemInform 41, no. 36 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.201036116.
Повний текст джерелаMehrabi, Tahmineh, and Alireza Ariafard. "The different roles of a cationic gold(i) complex in catalysing hydroarylation of alkynes and alkenes with a heterocycle." Chemical Communications 52, no. 60 (2016): 9422–25. http://dx.doi.org/10.1039/c6cc04370d.
Повний текст джерелаYamamoto, Yoshihiko. "Synthesis of heterocycles via transition-metal-catalyzed hydroarylation of alkynes." Chem. Soc. Rev. 43, no. 5 (2014): 1575–600. http://dx.doi.org/10.1039/c3cs60369e.
Повний текст джерелаLin, Baoda, Miaochang Liu, Zhishi Ye, Qin Zhang, and Jiang Cheng. "Rhodium–copper–TBAF-catalyzed hydroarylation of alkynes with aryl Trimethoxysilanes." Tetrahedron Letters 50, no. 15 (April 2009): 1714–16. http://dx.doi.org/10.1016/j.tetlet.2009.01.130.
Повний текст джерелаNagamoto, Midori, Jun-ichi Fukuda, Miyuki Hatano, Hideki Yorimitsu, and Takahiro Nishimura. "Hydroxoiridium-Catalyzed Hydroarylation of Alkynes and Bicycloalkenes with N-Sulfonylbenzamides." Organic Letters 19, no. 21 (October 19, 2017): 5952–55. http://dx.doi.org/10.1021/acs.orglett.7b02950.
Повний текст джерелаYoshikai, N., K. Gao, P. S. Lee, and T. Fujita. "Cobalt-Catalyzed Hydroarylation of Alkynes Through C-H Bond Activation." Synfacts 2010, no. 12 (November 22, 2010): 1410. http://dx.doi.org/10.1055/s-0030-1258858.
Повний текст джерелаXu, Xiaoling, Jiuxi Chen, Wenxia Gao, Huayue Wu, Jinchang Ding, and Weike Su. "ChemInform Abstract: Palladium-Catalyzed Hydroarylation of Alkynes with Arylboronic Acids." ChemInform 41, no. 33 (July 24, 2010): no. http://dx.doi.org/10.1002/chin.201033043.
Повний текст джерелаShaikh, Aslam C., S. Shalini, Ramanathan Vaidhyanathan, Manoj V. Mane, Ayan Kumar Barui, Chitta Ranjan Patra, Yeduru Venkatesh, Prakriti Ranjan Bangal, and Nitin T. Patil. "Identifying Solid Luminogens through Gold-Catalysed Intramolecular Hydroarylation of Alkynes." European Journal of Organic Chemistry 2015, no. 22 (June 30, 2015): 4860–67. http://dx.doi.org/10.1002/ejoc.201500503.
Повний текст джерелаBorsini, Elena, Gianluigi Broggini, Andrea Fasana, Chiara Baldassarri, Angelo M. Manzo, and Alcide D. Perboni. "Access to pyrrolo-pyridines by gold-catalyzed hydroarylation of pyrroles tethered to terminal alkynes." Beilstein Journal of Organic Chemistry 7 (October 26, 2011): 1468–74. http://dx.doi.org/10.3762/bjoc.7.170.
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