Статті в журналах з теми "Catalytic C-H"
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Hilinski, Michael, Shea Johnson, and Logan Combee. "Organocatalytic Atom-Transfer C(sp3)–H Oxidation." Synlett 29, no. 18 (June 27, 2018): 2331–36. http://dx.doi.org/10.1055/s-0037-1610432.
Повний текст джерелаZhang, Hua, and Li Wang. "Metal-Free Catalytic Aromatic C–H Borylation." Synlett 31, no. 19 (August 11, 2020): 1857–61. http://dx.doi.org/10.1055/s-0040-1707241.
Повний текст джерелаKakiuchi, Fumitoshi, and Shinji Murai. "Catalytic C−H/Olefin Coupling." Accounts of Chemical Research 35, no. 10 (October 2002): 826–34. http://dx.doi.org/10.1021/ar960318p.
Повний текст джерелаMurai, S., F. Kakiuchi, S. Sekine, Y. Tanaka, Asayuki Kamatani, M. Sonoda, and Naoto Chatani. "Catalytic C-H/olefin coupling." Pure and Applied Chemistry 66, no. 7 (January 1, 1994): 1527–34. http://dx.doi.org/10.1351/pac199466071527.
Повний текст джерелаBach, T., A. Nörder, P. Herrmann, and E. Herdtweck. "Diastereoselective Catalytic C-H Amination." Synfacts 2010, no. 10 (September 22, 2010): 1141. http://dx.doi.org/10.1055/s-0030-1258647.
Повний текст джерелаChen, Qing-An, Wei-Song Zhang, and Yan-Cheng Hu. "Isoprene: A Promising Coupling Partner in C–H Functionalizations." Synlett 31, no. 17 (July 2, 2020): 1649–55. http://dx.doi.org/10.1055/s-0040-1707172.
Повний текст джерелаNishii, Yuji, and Masahiro Miura. "Construction of Benzo-Fused Polycyclic Heteroaromatic Compounds through Palladium-Catalyzed Intramolecular C-H/C-H Biaryl Coupling." Catalysts 13, no. 1 (December 22, 2022): 12. http://dx.doi.org/10.3390/catal13010012.
Повний текст джерелаCollet, Florence, Camille Lescot, Chungen Liang, and Philippe Dauban. "Studies in catalytic C–H amination involving nitrene C–H insertion." Dalton Transactions 39, no. 43 (2010): 10401. http://dx.doi.org/10.1039/c0dt00283f.
Повний текст джерелаBedford, Robin B., Charlotte J. Mitchell, and Ruth L. Webster. "Solvent free catalytic C–H functionalisation." Chemical Communications 46, no. 18 (2010): 3095. http://dx.doi.org/10.1039/c003074k.
Повний текст джерелаYoung, Andrew J., and M. Christina White. "Catalytic Intermolecular Allylic CH Alkylation." Journal of the American Chemical Society 130, no. 43 (October 29, 2008): 14090–91. http://dx.doi.org/10.1021/ja806867p.
Повний текст джерелаReed, Sean A., and M. Christina White. "Catalytic Intermolecular Linear Allylic C−H Amination via Heterobimetallic Catalysis." Journal of the American Chemical Society 130, no. 11 (March 2008): 3316–18. http://dx.doi.org/10.1021/ja710206u.
Повний текст джерелаFutatsugi, Kentaro. "Recent Progress in Catalytic C-H Aminations." Journal of Synthetic Organic Chemistry, Japan 66, no. 6 (2008): 629–30. http://dx.doi.org/10.5059/yukigoseikyokaishi.66.629.
Повний текст джерелаTosi, Eleonora, Renata Marcia de Figueiredo, and Jean-Marc Campagne. "Enantioselective Catalytic C-H Amidations: An Highlight." Catalysts 11, no. 4 (April 6, 2021): 471. http://dx.doi.org/10.3390/catal11040471.
Повний текст джерелаCollet, Florence, Camille Lescot, and Philippe Dauban. "Catalytic C–H amination: the stereoselectivity issue." Chemical Society Reviews 40, no. 4 (2011): 1926. http://dx.doi.org/10.1039/c0cs00095g.
Повний текст джерелаCheng, Chen, and John F. Hartwig. "Catalytic Silylation of Unactivated C–H Bonds." Chemical Reviews 115, no. 17 (February 25, 2015): 8946–75. http://dx.doi.org/10.1021/cr5006414.
Повний текст джерелаDoyle, Michael P., Richard Duffy, Maxim Ratnikov, and Lei Zhou. "Catalytic Carbene Insertion into C−H Bonds." Chemical Reviews 110, no. 2 (February 10, 2010): 704–24. http://dx.doi.org/10.1021/cr900239n.
Повний текст джерелаGephart, Raymond T., Daria L. Huang, Mae Joanne B. Aguila, Graham Schmidt, Andi Shahu, and Timothy H. Warren. "Catalytic CH Amination with Aromatic Amines." Angewandte Chemie 124, no. 26 (May 15, 2012): 6594–98. http://dx.doi.org/10.1002/ange.201201921.
Повний текст джерелаKakiuchi, Fumitoshi, and Shinji Murai. "ChemInform Abstract: Catalytic C-H/Olefin Coupling." ChemInform 33, no. 51 (May 18, 2010): no. http://dx.doi.org/10.1002/chin.200251254.
Повний текст джерелаGephart, Raymond T., Daria L. Huang, Mae Joanne B. Aguila, Graham Schmidt, Andi Shahu, and Timothy H. Warren. "Catalytic CH Amination with Aromatic Amines." Angewandte Chemie International Edition 51, no. 26 (May 15, 2012): 6488–92. http://dx.doi.org/10.1002/anie.201201921.
Повний текст джерелаMURAI, S., F. KAKIUCHI, S. SEKINE, Y. TANAKA, A. KAMATANI, M. SONODA, and N. CHATANI. "ChemInform Abstract: Catalytic C-H/Olefin Coupling." ChemInform 25, no. 42 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199442300.
Повний текст джерелаZhang, Lin, and En-Qing Gao. "Catalytic C(sp)-H carboxylation with CO2." Coordination Chemistry Reviews 486 (July 2023): 215138. http://dx.doi.org/10.1016/j.ccr.2023.215138.
Повний текст джерелаVöller, Jan-Stefan. "Catalytic borylation of tertiary C–H bonds." Nature Catalysis 6, no. 4 (April 26, 2023): 287. http://dx.doi.org/10.1038/s41929-023-00953-0.
Повний текст джерелаBähr, Susanne, and Martin Oestreich. "The electrophilic aromatic substitution approach to C–H silylation and C–H borylation." Pure and Applied Chemistry 90, no. 4 (March 28, 2018): 723–31. http://dx.doi.org/10.1515/pac-2017-0902.
Повний текст джерелаMango, Frank D., Daniel M. Jarvie, and Eleanor Herriman. "Natural catalytic activity in a marine shale for generating natural gas." Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 466, no. 2124 (April 21, 2010): 3527–37. http://dx.doi.org/10.1098/rspa.2010.0032.
Повний текст джерелаBenfatti, Fides, Montse Guiteras Capdevila, Luca Zoli, Elena Benedetto, and Pier Giorgio Cozzi. "Catalytic stereoselective benzylic C–H functionalizations by oxidative C–H activation and organocatalysis." Chemical Communications, no. 39 (2009): 5919. http://dx.doi.org/10.1039/b910185c.
Повний текст джерелаLee, Sun Hwa, Serge I. Gorelsky, and Georgii I. Nikonov. "Catalytic H/D Exchange of Unactivated Aliphatic C–H Bonds." Organometallics 32, no. 21 (October 9, 2013): 6599–604. http://dx.doi.org/10.1021/om4009372.
Повний текст джерелаMantry, Lusina, Rajaram Maayuri, Vikash Kumar, and Parthasarathy Gandeepan. "Photoredox catalysis in nickel-catalyzed C–H functionalization." Beilstein Journal of Organic Chemistry 17 (August 31, 2021): 2209–59. http://dx.doi.org/10.3762/bjoc.17.143.
Повний текст джерелаLi, Yanjun, Yan-Cheng Liou, Xinran Chen, and Lutz Ackermann. "Thioether-enabled palladium-catalyzed atroposelective C–H olefination for N–C and C–C axial chirality." Chemical Science 13, no. 14 (2022): 4088–94. http://dx.doi.org/10.1039/d2sc00748g.
Повний текст джерелаGuillemard, Lucas, and Joanna Wencel-Delord. "When metal-catalyzed C–H functionalization meets visible-light photocatalysis." Beilstein Journal of Organic Chemistry 16 (July 21, 2020): 1754–804. http://dx.doi.org/10.3762/bjoc.16.147.
Повний текст джерелаLi, Jing, Huanan Huang, Weihong Liang, Qun Gao, and Zheng Duan. "Catalytic C–H and C–S Bond Activation of Thiophenes." Organic Letters 15, no. 2 (December 28, 2012): 282–85. http://dx.doi.org/10.1021/ol303136x.
Повний текст джерелаBrunard, Erwan, Vincent Boquet, Elsa Van Elslande, Tanguy Saget, and Philippe Dauban. "Catalytic Intermolecular C(sp3)–H Amination: Selective Functionalization of Tertiary C–H Bonds vs Activated Benzylic C–H Bonds." Journal of the American Chemical Society 143, no. 17 (April 26, 2021): 6407–12. http://dx.doi.org/10.1021/jacs.1c03872.
Повний текст джерелаMa, Jun-An, and Shen Li. "Catalytic fluorination of unactivated C(sp3)–H bonds." Org. Chem. Front. 1, no. 6 (2014): 712–15. http://dx.doi.org/10.1039/c4qo00078a.
Повний текст джерелаDavies, Huw M. L., and Rohan E. J. Beckwith. "Catalytic Enantioselective C−H Activation by Means of Metal−Carbenoid-Induced C−H Insertion." Chemical Reviews 103, no. 8 (August 2003): 2861–904. http://dx.doi.org/10.1021/cr0200217.
Повний текст джерелаDavies, Huw M. L., Qihui Jin, Pingda Ren, and Andrey Yu Kovalevsky. "Catalytic Asymmetric Benzylic C−H Activation by Means of Carbenoid-Induced C−H Insertions." Journal of Organic Chemistry 67, no. 12 (June 2002): 4165–69. http://dx.doi.org/10.1021/jo016351t.
Повний текст джерелаAl-Fatesh, Ahmed, Kenit Acharya, Ahmed I. Osman, Ghzzai Almutairi, Anis Hamza Fakeeha, Ahmed Elhag Abasaeed, Yousef A. Al-Baqmaa, and Rawesh Kumar. "Kinetic Study of Zirconia-Alumina-Supported Ni-Fe Catalyst for Dry Reforming of Methane: Impact of Partial Pressure and Reaction Temperature." International Journal of Chemical Engineering 2023 (May 11, 2023): 1–11. http://dx.doi.org/10.1155/2023/8667432.
Повний текст джерелаGauchot, V., D. R. Sutherland, and A. L. Lee. "Dual gold and photoredox catalysed C–H activation of arenes for aryl–aryl cross couplings." Chemical Science 8, no. 4 (2017): 2885–89. http://dx.doi.org/10.1039/c6sc05469b.
Повний текст джерелаChiusoli, Gian Paolo, Marta Catellani, Mirco Costa, Elena Motti, Nicola Della Ca’, and Giovanni Maestri. "Catalytic C–C coupling through C–H arylation of arenes or heteroarenes." Coordination Chemistry Reviews 254, no. 5-6 (March 2010): 456–69. http://dx.doi.org/10.1016/j.ccr.2009.07.023.
Повний текст джерелаYan, Ming, Li-Wei Yang, Wen-Hao Hu, Fu-Yao Zhang, and Albert S. C. Chan. "ChemInform Abstract: Catalytic Asymmetric Formation of C-H and C-C Bonds." ChemInform 32, no. 23 (May 26, 2010): no. http://dx.doi.org/10.1002/chin.200123264.
Повний текст джерелаMonguchi, Daiki, Taiki Fujiwara, Hirotoshi Furukawa, and Atsunori Mori. "Direct Amination of Azoles via Catalytic C−H, N−H Coupling." Organic Letters 11, no. 7 (April 2, 2009): 1607–10. http://dx.doi.org/10.1021/ol900298e.
Повний текст джерелаMatsuda, Takanori. "Catalytic Functionalization of Unactivated sp3 C-H Bonds." Journal of Synthetic Organic Chemistry, Japan 64, no. 7 (2006): 780–81. http://dx.doi.org/10.5059/yukigoseikyokaishi.64.780.
Повний текст джерелаSantoro, Stefano, Sergei I. Kozhushkov, Lutz Ackermann, and Luigi Vaccaro. "Heterogeneous catalytic approaches in C–H activation reactions." Green Chemistry 18, no. 12 (2016): 3471–93. http://dx.doi.org/10.1039/c6gc00385k.
Повний текст джерелаBae, Seri, Ha-Lim Jang, Haeun Jung, and Jung Min Joo. "Catalytic C–H Allylation and Benzylation of Pyrazoles." Journal of Organic Chemistry 80, no. 1 (December 17, 2014): 690–97. http://dx.doi.org/10.1021/jo5025317.
Повний текст джерелаToutov, Anton A., Wen-Bo Liu, Kerry N. Betz, Brian M. Stoltz, and Robert H. Grubbs. "Catalytic C–H bond silylation of aromatic heterocycles." Nature Protocols 10, no. 12 (October 29, 2015): 1897–903. http://dx.doi.org/10.1038/nprot.2015.118.
Повний текст джерелаJohnson, S. A. "Nickel complexes for catalytic C–H bond functionalization." Dalton Transactions 44, no. 24 (2015): 10905–13. http://dx.doi.org/10.1039/c5dt00032g.
Повний текст джерелаXu, Liang, Guanghui Wang, Shuai Zhang, Hong Wang, Linghua Wang, Li Liu, Jiao Jiao, and Pengfei Li. "Recent advances in catalytic C−H borylation reactions." Tetrahedron 73, no. 51 (December 2017): 7123–57. http://dx.doi.org/10.1016/j.tet.2017.11.005.
Повний текст джерелаHuang, Xiongyi, and John T. Groves. "Taming Azide Radicals for Catalytic C–H Azidation." ACS Catalysis 6, no. 2 (December 31, 2015): 751–59. http://dx.doi.org/10.1021/acscatal.5b02474.
Повний текст джерелаBedford, Robin B., Charlotte J. Mitchell, and Ruth L. Webster. "ChemInform Abstract: Solvent-Free Catalytic C-H Functionalization." ChemInform 41, no. 38 (August 26, 2010): no. http://dx.doi.org/10.1002/chin.201038085.
Повний текст джерелаBadiei, Yosra M, Adriana Dinescu, Xuliang Dai, Robert M Palomino, Frank W Heinemann, Thomas R Cundari, and Timothy H Warren. "Copper-Nitrene Complexes in Catalytic CH Amination." Angewandte Chemie International Edition 47, no. 51 (December 8, 2008): 9961–64. http://dx.doi.org/10.1002/anie.200804304.
Повний текст джерелаBadiei, Yosra M, Adriana Dinescu, Xuliang Dai, Robert M Palomino, Frank W Heinemann, Thomas R Cundari, and Timothy H Warren. "Copper-Nitrene Complexes in Catalytic CH Amination." Angewandte Chemie 120, no. 51 (December 8, 2008): 10109–12. http://dx.doi.org/10.1002/ange.200804304.
Повний текст джерелаTomin, Anna, Seema Bag, and Bela Torok. "ChemInform Abstract: Catalytic C-H Bond Activation Reactions." ChemInform 44, no. 18 (April 11, 2013): no. http://dx.doi.org/10.1002/chin.201318231.
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