Статті в журналах з теми "Formation de liaisons C-S"
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Top, Siden, and Gérard Jaouen. "Formation de liaison CC par couplage réducteur d'ions carbéniums arène chrome tricarbonyle." Journal of Organometallic Chemistry 336, no. 1-2 (December 1987): 143–51. http://dx.doi.org/10.1016/0022-328x(87)87164-4.
Повний текст джерелаHiemstra, Henk, Floris P. Rutjes, Sape S. Kinderman, Jan H. van Maarseveen, and Hans E. Schoemaker. "C-C Bond Formation viaN-Phosphoryliminium Ions." Synthesis 2004, no. 09 (2004): 1413–18. http://dx.doi.org/10.1055/s-2004-822376.
Повний текст джерелаPeng, Kang, Hui Zhu, Xing Liu, Han-Ying Peng, Jin-Quan Chen, and Zhi-Bing Dong. "Chemoselective C-S/S-S Formation between Diaryl Disulfides and Tetraalkylthiuram Disulfides." European Journal of Organic Chemistry 2019, no. 47 (November 27, 2019): 7629–34. http://dx.doi.org/10.1002/ejoc.201901401.
Повний текст джерелаMarkó, István E., J. Mike Southern, and M. Lakshmi Kantam. "Stoichiometric C-C Bond Formation Using Triorganothallium Reagents." Synlett 1991, no. 04 (1991): 235–37. http://dx.doi.org/10.1055/s-1991-20690.
Повний текст джерелаWang, Haibo, Lu Wang, Jinsai Shang, Xing Li, Haoyuan Wang, Jie Gui, and Aiwen Lei. "Fe-catalysed oxidative C–H functionalization/C–S bond formation." Chem. Commun. 48, no. 1 (2012): 76–78. http://dx.doi.org/10.1039/c1cc16184a.
Повний текст джерелаSharma, Upendra, Ritika Sharma, Rakesh Kumar, Inder Kumar, and Bikram Singh. "Selective C–Si Bond Formation through C–H Functionalization." Synthesis 47, no. 16 (July 9, 2015): 2347–66. http://dx.doi.org/10.1055/s-0034-1380435.
Повний текст джерелаZhang, Honghua, Huihong Wang, Yi Jiang, Fei Cao, Weiwei Gao, Longqing Zhu, Yuhang Yang, et al. "Recent Advances in Iodine‐Promoted C−S/N−S Bonds Formation." Chemistry – A European Journal 26, no. 72 (October 5, 2020): 17289–317. http://dx.doi.org/10.1002/chem.202001414.
Повний текст джерелаSun, Fengli, Xuemin Liu, Xinzhi Chen, Chao Qian, and Xin Ge. "Progress in the Formation of C-S Bond." Chinese Journal of Organic Chemistry 37, no. 9 (2017): 2211. http://dx.doi.org/10.6023/cjoc201703038.
Повний текст джерелаJean, Mickaël, Jacques Renault, Pierre van de Weghe, and Naoki Asao. "Gold-catalyzed C–S bond formation from thiols." Tetrahedron Letters 51, no. 2 (January 2010): 378–81. http://dx.doi.org/10.1016/j.tetlet.2009.11.025.
Повний текст джерелаChoudhuri, Khokan, Milan Pramanik, and Prasenjit Mal. "Noncovalent Interactions in C–S Bond Formation Reactions." Journal of Organic Chemistry 85, no. 19 (August 25, 2020): 11997–2011. http://dx.doi.org/10.1021/acs.joc.0c01534.
Повний текст джерелаAitken, R. Alan, Clémence Hauduc, M. Selim Hossain, Emily McHale, Adrian L. Schwan, Alexandra M. Z. Slawin, and Colin A. Stewart. "Unexpected Pyrolytic Behaviour of Substituted Benzo[c]thiopyran and Thieno[2,3-c]thiopyran S,S-dioxides." Australian Journal of Chemistry 67, no. 9 (2014): 1288. http://dx.doi.org/10.1071/ch14155.
Повний текст джерелаShi, Z., S. Yang, B. Li, and X. Wan. "C-H Functionalization via C-H Activation and C-C Bond Formation with Arylsilanes." Synfacts 2007, no. 7 (July 2007): 0751. http://dx.doi.org/10.1055/s-2007-968643.
Повний текст джерелаSong, Chunlan, Kun Liu, Xin Dong, Chien-Wei Chiang, and Aiwen Lei. "Recent Advances in Electrochemical Oxidative Cross-Coupling for the Construction of C–S Bonds." Synlett 30, no. 10 (April 15, 2019): 1149–63. http://dx.doi.org/10.1055/s-0037-1611753.
Повний текст джерелаKaur, Navjeet. "Cobalt-catalyzed C–N, C–O, C–S bond formation: synthesis of heterocycles." Journal of the Iranian Chemical Society 16, no. 12 (July 6, 2019): 2525–53. http://dx.doi.org/10.1007/s13738-019-01731-1.
Повний текст джерелаMejía, Esteban, and Ahmad A. Almasalma. "Recent Advances on Copper-Catalyzed C–C Bond Formation via C–H Functionalization." Synthesis 52, no. 18 (May 19, 2020): 2613–22. http://dx.doi.org/10.1055/s-0040-1707815.
Повний текст джерелаBhunia, Subhajit, Govind Goroba Pawar, S. Vijay Kumar, Yongwen Jiang, and Dawei Ma. "Selected Copper-Based Reactions for C−N, C−O, C−S, and C−C Bond Formation." Angewandte Chemie International Edition 56, no. 51 (November 15, 2017): 16136–79. http://dx.doi.org/10.1002/anie.201701690.
Повний текст джерелаMitrofanov, Alexander Yu, Arina V. Murashkina, Iris Martín-García, Francisco Alonso, and Irina P. Beletskaya. "Formation of C–C, C–S and C–N bonds catalysed by supported copper nanoparticles." Catalysis Science & Technology 7, no. 19 (2017): 4401–12. http://dx.doi.org/10.1039/c7cy01343d.
Повний текст джерелаZhao, Binlin, Torben Rogge, Lutz Ackermann, and Zhuangzhi Shi. "Metal-catalysed C–Het (F, O, S, N) and C–C bond arylation." Chemical Society Reviews 50, no. 16 (2021): 8903–53. http://dx.doi.org/10.1039/c9cs00571d.
Повний текст джерелаWang, G. W., T. T. Yuan, and D. D. Li. "Palladium-Catalyzed One-Pot C-C and C-N Bond Formation by Dual C-H Activation." Synfacts 2011, no. 07 (June 17, 2011): 0808. http://dx.doi.org/10.1055/s-0030-1260671.
Повний текст джерелаBroniowska, Katarzyna A., Agnes Keszler, Swati Basu, Daniel B. Kim-Shapiro, and Neil Hogg. "Cytochrome c-mediated formation of S-nitrosothiol in cells." Biochemical Journal 442, no. 1 (January 27, 2012): 191–97. http://dx.doi.org/10.1042/bj20111294.
Повний текст джерелаJung, K., K. Yoo, and C. Yoon. "Highly Efficient Pd-Catalyzed Oxidative sp2-sp2 C-C Bond Formation." Synfacts 2007, no. 3 (March 2007): 0301. http://dx.doi.org/10.1055/s-2007-968179.
Повний текст джерелаBasak, Amit, Sayantan Mondal, Tapobrata Mitra, Raja Mukherjee, and Partha Addy. "Garratt–Braverman Cyclization, a Powerful Tool for C–C Bond Formation." Synlett 23, no. 18 (October 19, 2012): 2582–602. http://dx.doi.org/10.1055/s-0032-1317321.
Повний текст джерелаYoshikai, Naohiko. "Recent Advances in Enantioselective C–C Bond Formation via Organocobalt Species." Synthesis 51, no. 01 (December 3, 2018): 135–45. http://dx.doi.org/10.1055/s-0037-1610397.
Повний текст джерелаWang, Congyang. "Manganese-Mediated C-C Bond Formation via C-H Activation: From Stoichiometry to Catalysis." Synlett 24, no. 13 (July 11, 2013): 1606–13. http://dx.doi.org/10.1055/s-0033-1339299.
Повний текст джерелаModha, Sachin G., Vaibhav P. Mehta, and Erik V. Van der Eycken. "Transition metal-catalyzed C–C bond formation via C–S bond cleavage: an overview." Chemical Society Reviews 42, no. 12 (2013): 5042. http://dx.doi.org/10.1039/c3cs60041f.
Повний текст джерелаWang, Haibo, Lu Wang, Jinsai Shang, Xing Li, Haoyuan Wang, Jie Gui, and Aiwen Lei. "ChemInform Abstract: Fe-Catalyzed Oxidative C-H Functionalization/C-S Bond Formation." ChemInform 43, no. 16 (March 22, 2012): no. http://dx.doi.org/10.1002/chin.201216130.
Повний текст джерелаNgo, Thi-Thuy-Duong, Thi-Huong Nguyen, Chloée Bournaud, Régis Guillot, Martial Toffano, and Giang Vo-Thanh. "Phosphine-Thiourea-Organocatalyzed Asymmetric C−N and C−S Bond Formation Reactions." Asian Journal of Organic Chemistry 5, no. 7 (May 30, 2016): 895–99. http://dx.doi.org/10.1002/ajoc.201600212.
Повний текст джерелаBorpatra, Paran J., Bhaskar Deka, Mohit L. Deb, and Pranjal K. Baruah. "Recent advances in intramolecular C–O/C–N/C–S bond formation via C–H functionalization." Organic Chemistry Frontiers 6, no. 20 (2019): 3445–89. http://dx.doi.org/10.1039/c9qo00863b.
Повний текст джерелаYeung, Ying-Yeung, and Jonathan Wong. "Recent Advances in C–Br Bond Formation." Synlett 32, no. 13 (April 16, 2021): 1354–64. http://dx.doi.org/10.1055/s-0037-1610772.
Повний текст джерелаSundaravelu, Nallappan, Subramani Sangeetha, and Govindasamy Sekar. "Metal-catalyzed C–S bond formation using sulfur surrogates." Organic & Biomolecular Chemistry 19, no. 7 (2021): 1459–82. http://dx.doi.org/10.1039/d0ob02320e.
Повний текст джерелаPrabhu, Achutha, Jorge S. Dolado, Eddie A. B. Koenders, Rafael Zarzuela, María J. Mosquera, Ines Garcia-Lodeiro, and María Teresa Blanco-Varela. "A patchy particle model for C-S-H formation." Cement and Concrete Research 152 (February 2022): 106658. http://dx.doi.org/10.1016/j.cemconres.2021.106658.
Повний текст джерелаHuang, Zhiliang, Dongchao Zhang, Xiaotian Qi, Zhiyuan Yan, Mengfan Wang, Haiming Yan, and Aiwen Lei. "Radical–Radical Cross-Coupling for C–S Bond Formation." Organic Letters 18, no. 10 (May 6, 2016): 2351–54. http://dx.doi.org/10.1021/acs.orglett.6b00764.
Повний текст джерелаSuzuki, Kazutaka, Tadahiro Nishikawa, and Suketoshi Ito. "Formation and carbonation of C-S-H in water." Cement and Concrete Research 15, no. 2 (March 1985): 213–24. http://dx.doi.org/10.1016/0008-8846(85)90032-8.
Повний текст джерелаBroniowska, Katarzyna A., Agnes Keszler, Swati Basu, Daniel B. Kim-Shapiro, and Neil Hogg. "Cytochrome C-Mediated Formation of S-Nitrosothiol in Cells." Free Radical Biology and Medicine 51 (November 2011): S156. http://dx.doi.org/10.1016/j.freeradbiomed.2011.10.208.
Повний текст джерелаLi, Jianxiao, Shaorong Yang, Wanqing Wu, and Huanfeng Jiang. "Recent developments in palladium-catalyzed C–S bond formation." Organic Chemistry Frontiers 7, no. 11 (2020): 1395–417. http://dx.doi.org/10.1039/d0qo00377h.
Повний текст джерелаBahekar, Sushilkumar S., Aniket P. Sarkate, Vijay M. Wadhai, Pravin S. Wakte, and Devanand B. Shinde. "CuI catalyzed C S bond formation by using nitroarenes." Catalysis Communications 41 (November 2013): 123–25. http://dx.doi.org/10.1016/j.catcom.2013.07.019.
Повний текст джерелаManzano, H., A. Ayuela, and J. S. Dolado. "On the formation of cementitious C–S–H nanoparticles." Journal of Computer-Aided Materials Design 14, no. 1 (January 23, 2007): 45–51. http://dx.doi.org/10.1007/s10820-006-9030-0.
Повний текст джерелаXu, Yulong, Xiaonan Shi, and Lipeng Wu. "tBuOK-triggered bond formation reactions." RSC Advances 9, no. 41 (2019): 24025–29. http://dx.doi.org/10.1039/c9ra04242c.
Повний текст джерелаPeng, Kang, Ming-Yuan Gao, Yu-Yan Yi, Jia Guo, and Zhi-Bing Dong. "Copper/Nickel-Catalyzed Selective C-S/S-S Bond Formation Starting from O -Alkyl Phenylcarbamothioates." European Journal of Organic Chemistry 2020, no. 11 (March 11, 2020): 1665–72. http://dx.doi.org/10.1002/ejoc.201901884.
Повний текст джерелаXu, Jian, Fan Zhang, Shifan Zhang, Li Zhang, Xiaoxia Yu, Jianxiang Yan, and Qiuling Song. "Radical Promoted C(sp2)–S Formation and C(sp3)–S Bond Cleavage: Access to 2-Substituted Thiochromones." Organic Letters 21, no. 4 (January 28, 2019): 1112–15. http://dx.doi.org/10.1021/acs.orglett.9b00023.
Повний текст джерелаZhang, Ning, Lingling Miao, Yu Yang, Guohang Duan, Linlin Shi, Xin‐Qi Hao, Mao‐Ping Song, Yan Xu, and Xinju Zhu. "Assembly of Highly Functionalized Allylic Sulfones via a Stereoselective Pd‐Catalyzed Sequential C−C/C−S Cleavage and C−S Formation Process." ChemistrySelect 6, no. 19 (May 17, 2021): 4736–40. http://dx.doi.org/10.1002/slct.202101190.
Повний текст джерелаGao, Jian, Jie Feng, and Ding Du. "Shining Light on C−S Bonds: Recent Advances in C−C Bond Formation Reactions via C−S Bond Cleavage under Photoredox Catalysis." Chemistry – An Asian Journal 15, no. 22 (October 14, 2020): 3637–59. http://dx.doi.org/10.1002/asia.202000905.
Повний текст джерелаNúñez, Oswaldo, José Rodríguez, and Larry Angulo. "Kinetic study of the formation and rupture of stable tetrahedral intermediates. CO, CN and CS bond formation." Journal of Physical Organic Chemistry 7, no. 2 (February 1994): 80–89. http://dx.doi.org/10.1002/poc.610070205.
Повний текст джерелаAmekura, H., K. Narumi, A. Chiba, Y. Hirano, K. Yamada, S. Yamamoto, N. Ishikawa, N. Okubo, M. Toulemonde, and Y. Saitoh. "Mechanism of ion track formation in silicon by much lower energy deposition than the formation threshold." Physica Scripta 98, no. 4 (March 6, 2023): 045701. http://dx.doi.org/10.1088/1402-4896/acbbf5.
Повний текст джерелаHesse, Stéphanie, та Gilbert Kirsch. "Palladium-Catalyzed C-C Bond Formation from β-Chloroacroleins in Aqueous Media". Synthesis 2001, № 05 (2001): 0755–58. http://dx.doi.org/10.1055/s-2001-12775.
Повний текст джерелаMacabeo, Allan. "Synthetic Uses of Chlorotitanium(IV) Triisopropoxide in C-C(N) Bond Formation." Synlett 2008, no. 20 (November 24, 2008): 3247–48. http://dx.doi.org/10.1055/s-0028-1083139.
Повний текст джерелаSieber, Joshua D., and Toolika Agrawal. "Recent Developments in C–C Bond Formation Using Catalytic Reductive Coupling Strategies." Synthesis 52, no. 18 (May 25, 2020): 2623–38. http://dx.doi.org/10.1055/s-0040-1707128.
Повний текст джерелаHaag, Rainer, Dietmar Kuck, Xiao-Yong Fu, James M. Cook, and Armin de Meijere. "Facile Formation of Dihydroacepentalenediide fromcentro-Substituted Tribenzotriquinacenes with C-C Bond Cleavage." Synlett 1994, no. 05 (1994): 340–42. http://dx.doi.org/10.1055/s-1994-22846.
Повний текст джерелаKobayashi, S., U. Schneider, and H. Dao. "Indium(I)-Catalyzed C-C Bond Formation between Allyl Boronates and Acetals." Synfacts 2010, no. 09 (August 23, 2010): 1055. http://dx.doi.org/10.1055/s-0030-1257900.
Повний текст джерелаFlood, Dillon T., Xuejing Zhang, Xiang Fu, Zhenxiang Zhao, Shota Asai, Brittany B. Sanchez, Emily J. Sturgell, et al. "RASS‐Enabled S/P−C and S−N Bond Formation for DEL Synthesis." Angewandte Chemie 132, no. 19 (March 11, 2020): 7447–53. http://dx.doi.org/10.1002/ange.201915493.
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