Статті в журналах з теми "Heck-type reaction"
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Kurandina, Daria, Padon Chuentragool, and Vladimir Gevorgyan. "Transition-Metal-Catalyzed Alkyl Heck-Type Reactions." Synthesis 51, no. 05 (February 7, 2019): 985–1005. http://dx.doi.org/10.1055/s-0037-1611659.
Повний текст джерелаZhou, Huan, Liang Ge, Jinshuai Song, Wujun Jian, Yajun Li, Chunsen Li, and Hongli Bao. "HOTf-Catalyzed Alkyl-Heck-type Reaction." iScience 3 (May 2018): 255–63. http://dx.doi.org/10.1016/j.isci.2018.04.020.
Повний текст джерелаLee, A. L. "Enantioselective oxidative boron Heck reactions." Organic & Biomolecular Chemistry 14, no. 24 (2016): 5357–66. http://dx.doi.org/10.1039/c5ob01984b.
Повний текст джерелаWang, Sa-Sa, and Guo-Yu Yang. "Recent developments in low-cost TM-catalyzed Heck-type reactions (TM = transition metal, Ni, Co, Cu, and Fe)." Catalysis Science & Technology 6, no. 9 (2016): 2862–76. http://dx.doi.org/10.1039/c5cy02235e.
Повний текст джерелаNewman, Stephen, and Jaya Vandavasi. "A High-Throughput Approach to Discovery: Heck-Type Reactivity with Aldehydes." Synlett 29, no. 16 (June 12, 2018): 2081–86. http://dx.doi.org/10.1055/s-0037-1610161.
Повний текст джерелаZhu, Xiaoyan, Feng Liu, Xinwu Ba, and Yonggang Wu. "Tandem Suzuki Polymerization/Heck Cyclization Reaction to Form Ladder-Type 9,9′-Bifluorenylidene-Based Conjugated Polymer." Polymers 15, no. 16 (August 10, 2023): 3360. http://dx.doi.org/10.3390/polym15163360.
Повний текст джерелаHelaja, Juho, and Richard Göttlich. "A new catalytic hetero-Heck type reaction." Chemical Communications, no. 7 (March 6, 2002): 720–21. http://dx.doi.org/10.1039/b201209j.
Повний текст джерелаPirisedigh, Azadeh, Amin Zarei, Hojjat Seyedjamali, Leila Khazdooz, and Abdol R. Hajipour. "Heck-type reaction of aryldiazonium silica sulfates." Monatshefte für Chemie - Chemical Monthly 143, no. 5 (September 23, 2011): 791–95. http://dx.doi.org/10.1007/s00706-011-0632-1.
Повний текст джерелаKitamura, Tsugio, and Yuzo Fujiwara. "ChemInform Abstract: Dehydrogenative Heck-Type Reactions: The Fujiwara-Moritani Reaction." ChemInform 46, no. 15 (March 26, 2015): no. http://dx.doi.org/10.1002/chin.201515342.
Повний текст джерелаTeng, Shenghan, Malcolm E. Tessensohn, Richard D. Webster, and Jianrong Steve Zhou. "Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides." ACS Catalysis 8, no. 8 (July 2, 2018): 7439–44. http://dx.doi.org/10.1021/acscatal.8b02029.
Повний текст джерелаKURIHARA, Yuji, Mikiko SODEOKA, and Masakatsu SHIBASAKI. "Asymmetric Heck-Type Reaction Utilizing Hypervalent Alkenyliodonium Salt." CHEMICAL & PHARMACEUTICAL BULLETIN 42, no. 11 (1994): 2357–59. http://dx.doi.org/10.1248/cpb.42.2357.
Повний текст джерелаShults, E. E. "Modification of Biologically Active Plant Metabolites Via the Transition Metal Catalyzed Reactions." Eurasian Chemico-Technological Journal 15, no. 3 (May 13, 2013): 175. http://dx.doi.org/10.18321/ectj221.
Повний текст джерелаHu, Fangdong, Ying Xia, Zhenxing Liu, Chen Ma, Yan Zhang, and Jianbo Wang. "Palladium-catalyzed three-component reaction of N-tosylhydrazone, norbornene and aryl halide." Org. Biomol. Chem. 12, no. 22 (2014): 3590–93. http://dx.doi.org/10.1039/c4ob00590b.
Повний текст джерелаLi, Lixin, Zhengguang Zhao, Jing Xu, Haotian Luo, Yong Li, Xiantao Ma, Lin Tang, Bo Ren, Xinhua Cao, and Yan-Na Ma. "Synthesis of remote fluoroalkylated alkenes by a palladium-catalyzed relay Heck-type reaction." Chemical Communications 56, no. 65 (2020): 9384–87. http://dx.doi.org/10.1039/c9cc10048b.
Повний текст джерелаFan, Tao, Wei-Dong Meng, and Xingang Zhang. "Palladium-catalyzed Heck-type reaction of secondary trifluoromethylated alkyl bromides." Beilstein Journal of Organic Chemistry 13 (December 6, 2017): 2610–16. http://dx.doi.org/10.3762/bjoc.13.258.
Повний текст джерелаOjha, Subhadra, and Niranjan Panda. "Pd-Catalyzed desulfitative arylation of olefins by N-methoxysulfonamide." Organic & Biomolecular Chemistry 20, no. 6 (2022): 1292–98. http://dx.doi.org/10.1039/d1ob02360h.
Повний текст джерелаXu, Ren-Rui, Wei Wang, Xinxin Qi, and Xiao-Feng Wu. "Palladium-catalyzed cascade Heck-type thiocarbonylation for the synthesis of functionalized thioesters." Organic Chemistry Frontiers 9, no. 5 (2022): 1417–21. http://dx.doi.org/10.1039/d2qo00096b.
Повний текст джерелаMao, Jiangang, Shuo-Qing Zhang, Bing-Feng Shi, and Weiliang Bao. "Palladium(0)-catalyzed cyclopropanation of benzyl bromides via C(sp3)–H bond activation." Chem. Commun. 50, no. 28 (2014): 3692–94. http://dx.doi.org/10.1039/c3cc49231a.
Повний текст джерелаDou, Yingchao, Liting Yang, Lu Zhang, Panke Zhang, Heng Li, and Guanyu Yang. "Palladium-catalyzed reductive Heck-type vinylative dearomatization of unfunctionalized halonaphthalene derivatives." RSC Advances 6, no. 102 (2016): 100632–35. http://dx.doi.org/10.1039/c6ra22310a.
Повний текст джерелаCheng, Jiang, Zhishi Ye, Fan Chen, Fang Luo, Wenhui Wang, Baoda Lin, and Xiaofei Jia. "Palladium-Catalyzed Mizoroki-Heck-Type Reaction of Aryl Trimethoxysilanes." Synlett 2009, no. 13 (July 16, 2009): 2198–200. http://dx.doi.org/10.1055/s-0029-1217571.
Повний текст джерелаYamashita, Hiroshi, Toshi-aki Kobayashi, Teruyuki Hayashi, and Masato Tanaka. "Heck-type Reaction of lodotrimethylsilane with Olefins Affording Alkenyltrimethylsilanes." Chemistry Letters 20, no. 5 (May 1991): 761–62. http://dx.doi.org/10.1246/cl.1991.761.
Повний текст джерелаDyker, Gerald, Peter Grundt, Hardy Markwitz, and Gerald Henkel. "Heck Reaction and Robinson-Type Annulation: A Versatile Combination." Journal of Organic Chemistry 63, no. 17 (August 1998): 6043–47. http://dx.doi.org/10.1021/jo9803535.
Повний текст джерелаKoike, Tooru, Xiaoli Du, Tomoyuki Sanada, Yasuaki Danda, and Atsunori Mori. "Iridium-Catalyzed Mizoroki–Heck-Type Reaction of Organosilicon Reagents." Angewandte Chemie International Edition 42, no. 1 (January 3, 2003): 89–92. http://dx.doi.org/10.1002/anie.200390061.
Повний текст джерелаShirakawa, Eiji, Xuejing Zhang, and Tamio Hayashi. "Mizoroki-Heck-Type Reaction Mediated by Potassium tert-Butoxide." Angewandte Chemie International Edition 50, no. 20 (April 6, 2011): 4671–74. http://dx.doi.org/10.1002/anie.201008220.
Повний текст джерелаKurahashi, Takuya, Hiroshi Shinokubo, and Atsuhiro Osuka. "Intermolecular Rhodium-Catalyzed Carbometalation/Heck-Type Reaction in Water." Angewandte Chemie 118, no. 38 (September 25, 2006): 6484–86. http://dx.doi.org/10.1002/ange.200602585.
Повний текст джерелаHelaja, Juho, and Richard Goettlich. "ChemInform Abstract: A New Catalytic hetero-Heck Type Reaction." ChemInform 33, no. 33 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200233157.
Повний текст джерелаShirakawa, Eiji, Xuejing Zhang, and Tamio Hayashi. "Mizoroki-Heck-Type Reaction Mediated by Potassium tert-Butoxide." Angewandte Chemie 123, no. 20 (April 6, 2011): 4767–70. http://dx.doi.org/10.1002/ange.201008220.
Повний текст джерелаKurahashi, Takuya, Hiroshi Shinokubo, and Atsuhiro Osuka. "Intermolecular Rhodium-Catalyzed Carbometalation/Heck-Type Reaction in Water." Angewandte Chemie International Edition 45, no. 38 (September 25, 2006): 6336–38. http://dx.doi.org/10.1002/anie.200602585.
Повний текст джерелаZheng, Meifang, Pengquan Chen, Wanqing Wu, and Huanfeng Jiang. "Palladium-catalyzed Heck-type reaction of oximes with allylic alcohols: synthesis of pyridines and azafluorenones." Chemical Communications 52, no. 1 (2016): 84–87. http://dx.doi.org/10.1039/c5cc06958k.
Повний текст джерелаGudeika, Dalius, Gjergji Sini, Vygintas Jankauskas, Galyna Sych, and Juozas V. Grazulevicius. "Synthesis and properties of the derivatives of triphenylamine and 1,8-naphthalimide with the olefinic linkages between chromophores." RSC Advances 6, no. 3 (2016): 2191–201. http://dx.doi.org/10.1039/c5ra24820e.
Повний текст джерелаZhang, Ji-Quan, Jun Cao, Wei Li, Shu-Min Li, Yong-Kang Li, Jian-Ta Wang, and Lei Tang. "Palladium/copper-catalyzed arylation of alkenes with N′-acyl arylhydrazines." New Journal of Chemistry 41, no. 2 (2017): 437–41. http://dx.doi.org/10.1039/c6nj03718f.
Повний текст джерелаKhodja, Walid, Alexandre Leclair, Jordi Rull-Barrull, Françoise Zammattio, Ksenia V. Kutonova, Marina E. Trusova, François-Xavier Felpin, and Mireia Rodriguez-Zubiri. "The promoting effect of pyridine ligands in the Pd-catalysed Heck–Matsuda reaction." New Journal of Chemistry 40, no. 10 (2016): 8855–62. http://dx.doi.org/10.1039/c6nj01717g.
Повний текст джерелаYuan, Kedong, Rui Sang, Jean-François Soulé, and Henri Doucet. "Desulfitative Pd-catalysed coupling reaction using benzenesulfonyl chlorides and enones as the coupling partners." Catalysis Science & Technology 5, no. 5 (2015): 2904–12. http://dx.doi.org/10.1039/c5cy00089k.
Повний текст джерелаMiyake, Junpei, Masahiro Watanabe, and Kenji Miyatake. "Intrapolymer Heck reaction for proton conductive ladder-type aromatic block copolymers." RSC Adv. 4, no. 40 (2014): 21049–53. http://dx.doi.org/10.1039/c4ra02582b.
Повний текст джерелаGao, Pei-Sen, Kan Zhang, Ming-Ming Yang, Shan Xu, Hua-Ming Sun, Jin-Lei Zhang, Zi-Wei Gao, Wei-Qiang Zhang, and Li-Wen Xu. "A robust multifunctional ligand-controlled palladium-catalyzed carbonylation reaction in water." Chemical Communications 54, no. 40 (2018): 5074–77. http://dx.doi.org/10.1039/c8cc00324f.
Повний текст джерелаLi, Chao-Jun, Jianlin Huang, Xi-Jie Dai, Haining Wang, Ning Chen, Wei Wei, Huiying Zeng, et al. "An Old Dog with New Tricks: Enjoin Wolff–Kishner Reduction for Alcohol Deoxygenation and C–C Bond Formations." Synlett 30, no. 13 (June 13, 2019): 1508–24. http://dx.doi.org/10.1055/s-0037-1611853.
Повний текст джерелаIkeda, Yousuke, Tomoaki Nakamura, Hideki Yorimitsu, and Koichiro Oshima. "Cobalt-Catalyzed Heck-Type Reaction of Alkyl Halides with Styrenes." Journal of the American Chemical Society 124, no. 23 (June 2002): 6514–15. http://dx.doi.org/10.1021/ja026296l.
Повний текст джерелаMatsude, Akihiro, Koji Hirano, and Masahiro Miura. "Palladium‐Catalyzed Intramolecular Mizoroki‐Heck‐Type Reaction of Diarylmethyl Carbonates." Advanced Synthesis & Catalysis 362, no. 3 (December 10, 2019): 518–22. http://dx.doi.org/10.1002/adsc.201901398.
Повний текст джерелаIkeda, Yousuke, Hideki Yorimitsu, Hiroshi Shinokubo, and Koichiro Oshima. "Cobalt-Mediated Mizoroki-Heck-Type Reaction of Epoxide with Styrene." Advanced Synthesis & Catalysis 346, no. 13-15 (December 2004): 1631–34. http://dx.doi.org/10.1002/adsc.200404074.
Повний текст джерелаKURIHARA, Y., M. SODEOKA, and M. SHIBASAKI. "ChemInform Abstract: Asymmetric Heck-Type Reaction Utilizing Hypervalent Alkenyliodonium Salt." ChemInform 26, no. 24 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199524108.
Повний текст джерелаYorimitsu, Hideki, and Koichiro Oshima. "New synthetic reactions catalyzed by cobalt complexes." Pure and Applied Chemistry 78, no. 2 (January 1, 2006): 441–49. http://dx.doi.org/10.1351/pac200678020441.
Повний текст джерелаZhang, Yong, Ya-Kui Sun, Ya-Ping Chang, Hui Shao, and Yu-Ming Zhao. "Palladium-catalyzed cascade carbonylative annulation between alkene-tethered aryl iodides and carbon monoxide." Chemical Communications 57, no. 57 (2021): 7023–26. http://dx.doi.org/10.1039/d1cc02217b.
Повний текст джерелаDziemidkiewicz, Anna, Martyna Pingot, and Magdalena Maciejewska. "METAL COMPLEXES AS NEW PRO-ECOLOGICAL CROSSLINKING AGENTS FOR CHLOROPRENE RUBBER BASED ON HECK COUPLING REACTION." Rubber Chemistry and Technology 92, no. 3 (July 1, 2019): 589–97. http://dx.doi.org/10.5254/rct.19.81465.
Повний текст джерелаNaik, Nilesh H., Tukaram D. Urmode, Arun K. Sikder, and Radhika S. Kusurkar. "Total Synthesis of Bouchardatine." Australian Journal of Chemistry 66, no. 9 (2013): 1112. http://dx.doi.org/10.1071/ch13331.
Повний текст джерелаTarnowicz-Ligus, Stanisława, and Anna Trzeciak. "Heck Transformations of Biological Compounds Catalyzed by Phosphine-Free Palladium." Molecules 23, no. 9 (September 1, 2018): 2227. http://dx.doi.org/10.3390/molecules23092227.
Повний текст джерелаGlorius, Frank. "Palladium-catalyzed Heck-type reaction of 2-chloro acetamides with olefins." Tetrahedron Letters 44, no. 30 (July 2003): 5751–54. http://dx.doi.org/10.1016/s0040-4039(03)01377-7.
Повний текст джерелаOhff, Manuela, Andreas Ohff, Milko E. van der Boom, and David Milstein. "Highly Active Pd(II) PCP-Type Catalysts for the Heck Reaction." Journal of the American Chemical Society 119, no. 48 (December 1997): 11687–88. http://dx.doi.org/10.1021/ja9729692.
Повний текст джерелаZong, Zhenzhen, Wenxiao Wang, Xiaohui Bai, Hui Xi, and Zhiping Li. "Manganese-Catalyzed Alkyl-Heck-Type Reaction via Oxidative Decarbonylation of Aldehydes." Asian Journal of Organic Chemistry 4, no. 7 (May 14, 2015): 622–25. http://dx.doi.org/10.1002/ajoc.201500148.
Повний текст джерелаShirakawa, Eiji, Xuejing Zhang, and Tamio Hayashi. "ChemInform Abstract: Mizoroki-Heck-Type Reaction Mediated by Potassium tert-Butoxide." ChemInform 42, no. 38 (August 25, 2011): no. http://dx.doi.org/10.1002/chin.201138100.
Повний текст джерелаBettadapur, Kiran R., Mahadev Sharanappa Sherikar, Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "RhIII -Catalyzed C−H Activation: Mizoroki-Heck-Type Reaction of Maleimides." Asian Journal of Organic Chemistry 7, no. 7 (May 30, 2018): 1338–42. http://dx.doi.org/10.1002/ajoc.201800193.
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