Статті в журналах з теми "C-S bond formation"
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Xu, 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 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 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 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 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 джерелаStenfors, Brock A., Richard J. Staples, Shannon M. Biros, and Felix N. Ngassa. "Crystal structure of 1-[(4-methylbenzene)sulfonyl]pyrrolidine." Acta Crystallographica Section E Crystallographic Communications 76, no. 3 (February 28, 2020): 452–55. http://dx.doi.org/10.1107/s205698902000208x.
Повний текст джерелаShen, Chao, Pengfei Zhang, Qiang Sun, Shiqiang Bai, T. S. Andy Hor, and Xiaogang Liu. "Recent advances in C–S bond formation via C–H bond functionalization and decarboxylation." Chemical Society Reviews 44, no. 1 (2015): 291–314. http://dx.doi.org/10.1039/c4cs00239c.
Повний текст джерелаSaidalimu, Ibrayim, Shugo Suzuki, Etsuko Tokunaga, and Norio Shibata. "Successive C–C bond cleavage, fluorination, trifluoromethylthio- and pentafluorophenylthiolation under metal-free conditions to provide compounds with dual fluoro-functionalization." Chemical Science 7, no. 3 (2016): 2106–10. http://dx.doi.org/10.1039/c5sc04208a.
Повний текст джерелаLv, Zongchao, Huamin Wang, Zhicong Quan, Yuan Gao, and Aiwen Lei. "Dioxygen-triggered oxidative cleavage of the C–S bond towards C–N bond formation." Chemical Communications 55, no. 82 (2019): 12332–35. http://dx.doi.org/10.1039/c9cc05707b.
Повний текст джерелаRen, Rongguo, Zhen Wu, and Chen Zhu. "Manganese-catalyzed regiospecific sp3C–S bond formation through C–C bond cleavage of cyclobutanols." Chemical Communications 52, no. 52 (2016): 8160–63. http://dx.doi.org/10.1039/c6cc01843b.
Повний текст джерелаGogoi, Prasanta, Bappi Paul, Sukanya Hazarika, and Pranjit Barman. "Gold nanoparticle catalyzed intramolecular C–S bond formation/C–H bond functionalization/cyclization cascades." RSC Advances 5, no. 71 (2015): 57433–36. http://dx.doi.org/10.1039/c5ra10885c.
Повний текст джерелаMorita, Iori, Takahiro Mori, Takaaki Mitsuhashi, Shotaro Hoshino, Yoshimasa Taniguchi, Takashi Kikuchi, Kei Nagae, et al. "Exploiting a C–N Bond Forming Cytochrome P450 Monooxygenase for C–S Bond Formation." Angewandte Chemie 132, no. 10 (January 23, 2020): 4017–22. http://dx.doi.org/10.1002/ange.201916269.
Повний текст джерелаMorita, Iori, Takahiro Mori, Takaaki Mitsuhashi, Shotaro Hoshino, Yoshimasa Taniguchi, Takashi Kikuchi, Kei Nagae, et al. "Exploiting a C–N Bond Forming Cytochrome P450 Monooxygenase for C–S Bond Formation." Angewandte Chemie International Edition 59, no. 10 (January 23, 2020): 3988–93. http://dx.doi.org/10.1002/anie.201916269.
Повний текст джерелаWang, Min, Zhoujie Xie, Shoubin Tang, Ee Ling Chang, Yue Tang, Zhengyan Guo, Yinglu Cui, Bian Wu, Tao Ye, and Yihua Chen. "Reductase of Mutanobactin Synthetase Triggers Sequential C–C Macrocyclization, C–S Bond Formation, and C–C Bond Cleavage." Organic Letters 22, no. 3 (January 9, 2020): 960–64. http://dx.doi.org/10.1021/acs.orglett.9b04501.
Повний текст джерелаModha, Sachin G., Vaibhav P. Mehta, and Erik V. Van der Eycken. "ChemInform Abstract: Transition Metal Catalyzed C-C Bond Formation via C-S Bond Cleavage: An Overview." ChemInform 44, no. 36 (August 15, 2013): no. http://dx.doi.org/10.1002/chin.201336215.
Повний текст джерелаYang, Daoshan, Kelu Yan, Wei Wei, Laijin Tian, Qinghe Li, Jinmao You, and Hua Wang. "Metal-free n-Et4NBr-catalyzed radical cyclization of disulfides and alkynes leading to benzothiophenes under mild conditions." RSC Adv. 4, no. 89 (2014): 48547–53. http://dx.doi.org/10.1039/c4ra08260e.
Повний текст джерелаAllen, F. H., C. M. Bird, R. S. Rowland, and P. R. Raithby. "Resonance-Induced Hydrogen Bonding at Sulfur Acceptors in R 1 R 2C=S and R 1CS2 − Systems." Acta Crystallographica Section B Structural Science 53, no. 4 (August 1, 1997): 680–95. http://dx.doi.org/10.1107/s0108768197002656.
Повний текст джерелаLiu, Zijian, Kunbing Ouyang, and Nianfa Yang. "The thiolation of pentafluorobenzene with disulfides by C–H, C–F bond activation and C–S bond formation." Organic & Biomolecular Chemistry 16, no. 6 (2018): 988–92. http://dx.doi.org/10.1039/c7ob02836a.
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 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 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 джерелаDong, Dao-Qing, Shuang-Hong Hao, Dao-Shan Yang, Li-Xia Li, and Zu-Li Wang. "Sulfenylation of C-H Bonds for C-S Bond Formation under Metal-Free Conditions." European Journal of Organic Chemistry 2017, no. 45 (August 28, 2017): 6576–92. http://dx.doi.org/10.1002/ejoc.201700853.
Повний текст джерелаZhao, Jian-Nan, Muzaffar Kayumov, Dong-Yu Wang, and Ao Zhang. "Transition-Metal-Free Aryl–Heteroatom Bond Formation via C–S Bond Cleavage." Organic Letters 21, no. 18 (August 29, 2019): 7303–6. http://dx.doi.org/10.1021/acs.orglett.9b02584.
Повний текст джерелаSun, Kai, Yunhe Lv, Zhonghong Zhu, Liping Zhang, Hankui Wu, Lin Liu, Yongqing Jiang, Beibei Xiao та Xin Wang. "Oxidative C–S bond cleavage reaction of DMSO for C–N and C–C bond formation: new Mannich-type reaction for β-amino ketones". RSC Advances 5, № 4 (2015): 3094–97. http://dx.doi.org/10.1039/c4ra14249g.
Повний текст джерелаLanzi, Matteo, Jérémy Merad, Dina V. Boyarskaya, Giovanni Maestri, Clémence Allain, and Géraldine Masson. "Visible-Light-Triggered C–C and C–N Bond Formation by C–S Bond Cleavage of Benzylic Thioethers." Organic Letters 20, no. 17 (August 16, 2018): 5247–50. http://dx.doi.org/10.1021/acs.orglett.8b02196.
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 джерелаZhang, Rui, Huaiwei Ding, Xiangling Pu, Zhiping Qian, and Yan Xiao. "Recent Advances in the Synthesis of Sulfides, Sulfoxides and Sulfones via C-S Bond Construction from Non-Halide Substrates." Catalysts 10, no. 11 (November 17, 2020): 1339. http://dx.doi.org/10.3390/catal10111339.
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 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 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 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 джерелаArisawa, Mieko, Kenji Fujimoto, Satoshi Morinaka, and Masahiko Yamaguchi. "Equilibrating C−S Bond Formation by C−H and S−S Bond Metathesis. Rhodium-Catalyzed Alkylthiolation Reaction of 1-Alkynes with Disulfides." Journal of the American Chemical Society 127, no. 35 (September 2005): 12226–27. http://dx.doi.org/10.1021/ja0527121.
Повний текст джерелаGogoi, Anupal, Srimanta Guin, Suresh Rajamanickam, Saroj Kumar Rout, and Bhisma K. Patel. "Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C–N Bond Over C–S Bond Formation." Journal of Organic Chemistry 80, no. 18 (September 9, 2015): 9016–27. http://dx.doi.org/10.1021/acs.joc.5b00956.
Повний текст джерелаShen, Chao, Pengfei Zhang, Qiang Sun, Shiqiang Bai, T. S. Andy Hor, and Xiaogang Liu. "ChemInform Abstract: Recent Advances in C-S Bond Formation via C-H Bond Functionalization and Decarboxylation." ChemInform 46, no. 15 (March 26, 2015): no. http://dx.doi.org/10.1002/chin.201515296.
Повний текст джерелаGogoi, Prasanta, Bappi Paul, Sukanya Hazarika, and Pranjit Barman. "ChemInform Abstract: Gold Nanoparticle Catalyzed Intramolecular C-S Bond Formation/C-H Bond Functionalization/Cyclization Cascades." ChemInform 46, no. 47 (November 2015): no. http://dx.doi.org/10.1002/chin.201547144.
Повний текст джерелаShin, Jeongcheol, Jiseon Lee, Jong-Min Suh, and Kiyoung Park. "Ligand-field transition-induced C–S bond formation from nickelacycles." Chemical Science 12, no. 48 (2021): 15908–15. http://dx.doi.org/10.1039/d1sc05113j.
Повний текст джерелаJegelka, Markus, and Bernd Plietker. "Selective C−S Bond Formation via Fe-Catalyzed Allylic Substitution." Organic Letters 11, no. 15 (August 6, 2009): 3462–65. http://dx.doi.org/10.1021/ol901297s.
Повний текст джерелаMitsudo, Koichi, Toki Yonezawa, Ren Matsuo, and Seiji Suga. "Electrochemical Intramolecular C–S Bond Formation Leading to Thienoacene Derivatives." ECS Meeting Abstracts MA2020-01, no. 43 (May 1, 2020): 2507. http://dx.doi.org/10.1149/ma2020-01432507mtgabs.
Повний текст джерелаChen, Lian, Ali Noory Fajer, Zhanibek Yessimbekov, Mosstafa Kazemi, and Masoud Mohammadi. "Diaryl sulfides synthesis: copper catalysts in C–S bond formation." Journal of Sulfur Chemistry 40, no. 4 (March 24, 2019): 451–68. http://dx.doi.org/10.1080/17415993.2019.1596268.
Повний текст джерелаSeleznev, A. A., D. P. Radchenko, S. I. Golubova, S. A. Safronov, and V. A. Navrotskiy. "SULFONYL CHLORIDES - NOVEL SOURCE OF FREE RADICALS." IZVESTIA VOLGOGRAD STATE TECHNICAL UNIVERSITY, no. 12(259) (December 21, 2021): 103–14. http://dx.doi.org/10.35211/1990-5297-2021-12-259-103-114.
Повний текст джерелаAllen, F. H., C. M. Bird, R. S. Rowland, and P. R. Raithby. "Hydrogen-Bond Acceptor and Donor Properties of Divalent Sulfur (Y-S-Z and R-S-H)." Acta Crystallographica Section B Structural Science 53, no. 4 (August 1, 1997): 696–701. http://dx.doi.org/10.1107/s0108768197002644.
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 джерелаAnand, Devireddy, Yuwei He, Linyong Li, and Lei Zhou. "A photocatalytic sp3 C–S, C–Se and C–B bond formation through C–C bond cleavage of cycloketone oxime esters." Organic & Biomolecular Chemistry 17, no. 3 (2019): 533–40. http://dx.doi.org/10.1039/c8ob02987c.
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.
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 International Edition 59, no. 19 (March 11, 2020): 7377–83. http://dx.doi.org/10.1002/anie.201915493.
Повний текст джерелаNgah, Nurziana, Nor Azanita Mohamed, Bohari M. Yamin, and Hamizah Mohd Zaki. "3-[3-(2-Fluorobenzoyl)thioureido]propionic acid." Acta Crystallographica Section E Structure Reports Online 70, no. 6 (May 24, 2014): o705. http://dx.doi.org/10.1107/s1600536814011404.
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