Статті в журналах з теми "Borylation reaction"
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Chattopadhyay, Buddhadeb, Mirja Md Mahamudul Hassan, Md Emdadul Hoque, Sayan Dey, Saikat Guria, and Brindaban Roy. "Iridium-Catalyzed Site-Selective Borylation of 8-Arylquinolines." Synthesis 53, no. 18 (May 11, 2021): 3333–42. http://dx.doi.org/10.1055/a-1506-3884.
Повний текст джерелаIwamoto, Hiroaki, Koji Kubota, Eiji Yamamoto, and Hajime Ito. "Copper(i)-catalyzed carbon–halogen bond-selective boryl substitution of alkyl halides bearing terminal alkene moieties." Chemical Communications 51, no. 47 (2015): 9655–58. http://dx.doi.org/10.1039/c5cc02760h.
Повний текст джерелаXie, Jian-bo, Jian Luo, Timothy R. Winn, David B. Cordes, and Guigen Li. "Group-assisted purification (GAP) chemistry for the synthesis of Velcade via asymmetric borylation of N-phosphinylimines." Beilstein Journal of Organic Chemistry 10 (March 31, 2014): 746–51. http://dx.doi.org/10.3762/bjoc.10.69.
Повний текст джерелаLeon, Noel J., Hsien-Cheng Yu, Thomas J. Mazzacano, and Neal P. Mankad. "Pursuit of C–H Borylation Reactions with Non-Precious Heterobimetallic Catalysts: Hypothesis-Driven Variations on a Design Theme." Synlett 31, no. 02 (November 27, 2019): 125–32. http://dx.doi.org/10.1055/s-0039-1691504.
Повний текст джерелаBritton, Luke, Jamie H. Docherty, Andrew P. Dominey, and Stephen P. Thomas. "Iron-Catalysed C(sp2)-H Borylation Enabled by Carboxylate Activation." Molecules 25, no. 4 (February 18, 2020): 905. http://dx.doi.org/10.3390/molecules25040905.
Повний текст джерелаJi, Hong, Li-Yang Wu, Jiang-Hong Cai, Guo-Rong Li, Na-Na Gan, and Zhao-Hua Wang. "Room-temperature borylation and one-pot two-step borylation/Suzuki–Miyaura cross-coupling reaction of aryl chlorides." RSC Advances 8, no. 25 (2018): 13643–48. http://dx.doi.org/10.1039/c8ra01381k.
Повний текст джерелаPinet, Sandra, Mathieu Pucheault, Virginie Liautard, and Mégane Debiais. "Radical Metal-Free Borylation of Aryl Iodides." Synthesis 49, no. 21 (May 29, 2017): 4759–68. http://dx.doi.org/10.1055/s-0036-1588431.
Повний текст джерелаLi, Bingru, Huayu Liang, Arumugam Vignesh, Xiaoyu Zhou, Yan Liu, and Zhuofeng Ke. "Updated Progress of the Copper-Catalyzed Borylative Functionalization of Unsaturated Molecules." Molecules 28, no. 5 (February 28, 2023): 2252. http://dx.doi.org/10.3390/molecules28052252.
Повний текст джерелаGeier, Stephen J., and Stephen A. Westcott. "Dehydrogenative borylation: the dark horse in metal-catalyzed hydroborations and diborations?" Reviews in Inorganic Chemistry 35, no. 2 (June 1, 2015): 69–79. http://dx.doi.org/10.1515/revic-2014-0008.
Повний текст джерелаSteven, Alan. "Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates." Synthesis 51, no. 13 (May 21, 2019): 2632–47. http://dx.doi.org/10.1055/s-0037-1610714.
Повний текст джерелаRoesner, Stefan, and Varinder K. Aggarwal. "Enantioselective synthesis of (R)-tolterodine using lithiation/borylation–protodeboronation methodology." Canadian Journal of Chemistry 90, no. 11 (November 2012): 965–74. http://dx.doi.org/10.1139/v2012-069.
Повний текст джерелаCai, Mingzhong, Bin Huang, Chengkai Luo, and Caifeng Xu. "Recyclable Pd2dba3/XPhos/PEG-2000 System for Efficient Borylation of Aryl Chlorides: Practical Access to Aryl Boronates." Synthesis 54, no. 05 (November 22, 2021): 1339–46. http://dx.doi.org/10.1055/s-0037-1610787.
Повний текст джерелаLi, Dai-Yu, Rui-Mu Yu, Jin-Ping Li, Deng-Feng Yang, Qi Pang, and Hong-Liang Li. "The Improved para-Selective C(sp2)-H Borylation of Anisole Derivatives Enabled by Bulky Lewis Acid." Catalysts 13, no. 8 (August 9, 2023): 1193. http://dx.doi.org/10.3390/catal13081193.
Повний текст джерелаPan, Zilong, Luhua Liu, Senmiao Xu, and Zhenlu Shen. "Ligand-free iridium-catalyzed regioselective C–H borylation of indoles." RSC Advances 11, no. 10 (2021): 5487–90. http://dx.doi.org/10.1039/d0ra10211c.
Повний текст джерелаWelle, Alexandre, Virginie Cirriez, and Olivier Riant. "Copper catalyzed tandem conjugated borylation–aldol reaction." Tetrahedron 68, no. 17 (April 2012): 3435–43. http://dx.doi.org/10.1016/j.tet.2011.07.062.
Повний текст джерелаMotokura, Ken, and Kyogo Maeda. "Recent Advances in Heterogeneous Ir Complex Catalysts for Aromatic C–H Borylation." Synthesis 53, no. 18 (April 9, 2021): 3227–34. http://dx.doi.org/10.1055/a-1478-6118.
Повний текст джерелаPing, Yifan, Taiwei Chang, Kang Wang, Jingfeng Huo, and Jianbo Wang. "Palladium-catalyzed oxidative borylation of conjugated enynones through carbene migratory insertion: synthesis of furyl-substituted alkenylboronates." Chemical Communications 55, no. 1 (2019): 59–62. http://dx.doi.org/10.1039/c8cc09024f.
Повний текст джерелаLu, Haiyan, Xiumei Yang, Liwei Zhou, Wenguang Li, Guobo Deng, Yuan Yang, and Yun Liang. "Palladium-catalyzed domino Heck-disilylation and -borylation of alkene-tethered 2-(2-halophenyl)-1H-indoles: access to diverse disilylated and borylated indolo[2,1-a]isoquinolines." Organic Chemistry Frontiers 7, no. 15 (2020): 2016–21. http://dx.doi.org/10.1039/d0qo00492h.
Повний текст джерелаChen, You, Hui Peng, Yun-Xiao Pi, Tong Meng, Ze-Yu Lian, Meng-Qi Yan, Yan Liu, Sheng-Hua Liu, and Guang-Ao Yu. "Efficient phosphine ligands for the one-pot palladium-catalyzed borylation/Suzuki–Miyaura cross-coupling reaction." Organic & Biomolecular Chemistry 13, no. 11 (2015): 3236–42. http://dx.doi.org/10.1039/c4ob02436b.
Повний текст джерелаKidonakis, Marios, Michael Fragkiadakis та Manolis Stratakis. "β-Borylation of conjugated carbonyl compounds with silylborane or bis(pinacolato)diboron catalyzed by Au nanoparticles". Organic & Biomolecular Chemistry 18, № 43 (2020): 8921–27. http://dx.doi.org/10.1039/d0ob01806f.
Повний текст джерелаWang, Jianbo. "When diazo compounds meet with organoboron compounds." Pure and Applied Chemistry 90, no. 4 (March 28, 2018): 617–23. http://dx.doi.org/10.1515/pac-2017-0713.
Повний текст джерелаWu, Yuanqi, Lizuo Wu, Zhan-Ming Zhang, Bing Xu, Yu Liu, and Junliang Zhang. "Enantioselective difunctionalization of alkenes by a palladium-catalyzed Heck/borylation sequence." Chemical Science 13, no. 7 (2022): 2021–25. http://dx.doi.org/10.1039/d1sc06229h.
Повний текст джерелаYoshimura, Aya, Michiyo Yoshinaga, Hiroshi Yamashita, Masayasu Igarashi, Shigeru Shimada, and Kazuhiko Sato. "A convenient and clean synthetic method for borasiloxanes by Pd-catalysed reaction of silanols with diborons." Chemical Communications 53, no. 43 (2017): 5822–25. http://dx.doi.org/10.1039/c7cc02420g.
Повний текст джерелаYang, Shengbiao, and Juntao Ye. "Borylation of azines via a Minisci-type reaction." Chem 7, no. 7 (July 2021): 1703–5. http://dx.doi.org/10.1016/j.chempr.2021.06.013.
Повний текст джерелаKruppa, Marco, and Thomas J. J. Müller. "Masuda Borylation–Suzuki Coupling (MBSC) Sequence: A One-Pot Process to Access Complex (hetero)Biaryls." Catalysts 13, no. 2 (February 4, 2023): 350. http://dx.doi.org/10.3390/catal13020350.
Повний текст джерелаHale, Lillian V. A., David G. Emmerson, Emma F. Ling, Andrew J. Roering, Marissa A. Ringgold, and Timothy B. Clark. "An ortho-directed C–H borylation/Suzuki coupling sequence in the formation of biphenylbenzylic amines." Organic Chemistry Frontiers 2, no. 6 (2015): 661–64. http://dx.doi.org/10.1039/c4qo00348a.
Повний текст джерелаPujol, Alba, Adam D. J. Calow, Andrei S. Batsanov, and Andrew Whiting. "One-pot catalytic asymmetric borylation of unsaturated aldehyde-derived imines; functionalisation to homoallylic boronate carboxylate ester derivatives." Organic & Biomolecular Chemistry 13, no. 18 (2015): 5122–30. http://dx.doi.org/10.1039/c4ob02657h.
Повний текст джерелаFranco, Mario, Emily L. Vargas, Mariola Tortosa, and M. Belén Cid. "Coupling of thiols and aromatic halides promoted by diboron derived super electron donors." Chemical Communications 57, no. 88 (2021): 11653–56. http://dx.doi.org/10.1039/d1cc05294b.
Повний текст джерелаHu, Jiefeng, Matthias Ferger, Zhuangzhi Shi, and Todd B. Marder. "Recent advances in asymmetric borylation by transition metal catalysis." Chemical Society Reviews 50, no. 23 (2021): 13129–88. http://dx.doi.org/10.1039/d0cs00843e.
Повний текст джерелаFranco, Mario, Raquel Sainz, Al Mokhtar Lamsabhi, Cristina Díaz, Mariola Tortosa, and M. Belén Cid. "Evaluation of the role of graphene-based Cu(i) catalysts in borylation reactions." Catalysis Science & Technology 11, no. 10 (2021): 3501–13. http://dx.doi.org/10.1039/d1cy00104c.
Повний текст джерелаChen, Shuangshuang, Zhangjin Pan, and Yan Wang. "PPh3-Mediated Borylation of Arenediazonium Salts with Bis(pinacolato)diborane." Zeitschrift für Naturforschung B 69, no. 9-10 (October 1, 2014): 982–86. http://dx.doi.org/10.5560/znb.2014-4139.
Повний текст джерелаTsurugi, Hayato, Kazushi Mashima, Luis C. Misal Castro, and Ibrahim Sultan. "Pyridine-Mediated B–B Bond Activation of (RO)2B–B(OR)2 for Generating Borylpyridine Anions and Pyridine-Stabilized Boryl Radicals as Useful Boryl Reagents in Organic Synthesis." Synthesis 53, no. 18 (April 20, 2021): 3211–26. http://dx.doi.org/10.1055/a-1486-8169.
Повний текст джерелаYao, Zhengjie, Zhenwei Zhang, Jiali Li, Ji Jia, Si Ma, Yongfeng Zhi, Hong Xia та Xiaoming Liu. "Fully π-conjugated, diyne-linked covalent organic frameworks formed via alkyne–alkyne cross-coupling reaction". Materials Chemistry Frontiers 6, № 4 (2022): 466–72. http://dx.doi.org/10.1039/d1qm01322j.
Повний текст джерелаVan Hoveln, R. J., S. C. Schmid, M. Tretbar, C. T. Buttke, and J. M. Schomaker. "Formal asymmetric hydrobromination of styrenes via copper-catalyzed 1,3-halogen migration." Chem. Sci. 5, no. 12 (2014): 4763–67. http://dx.doi.org/10.1039/c4sc02040e.
Повний текст джерелаToyota, Kozo, Shinichi Mikami, Akihiro Matsuo, and Eunsang Kwon. "Synthesis of 4,7′-Bibenzo[b]thiophenes Bearing Several Different Substituents at 2-, 2′-, 4′-, and 7-Positions; Structurally Featured Molecular Scaffolds for Selective Substitution." Synlett 32, no. 18 (September 28, 2021): 1826–32. http://dx.doi.org/10.1055/s-0040-1719839.
Повний текст джерелаZhang, Yahui, Xiangyu Zhao, Ce Bi, Wenqi Lu, Mengyuan Song, Dongdong Wang, and Guangyan Qing. "Selective electrocatalytic hydroboration of aryl alkenes." Green Chemistry 23, no. 4 (2021): 1691–99. http://dx.doi.org/10.1039/d0gc03890c.
Повний текст джерелаHuang, Genping, Marcin Kalek, Rong-Zhen Liao, and Fahmi Himo. "Mechanism, reactivity, and selectivity of the iridium-catalyzed C(sp3)–H borylation of chlorosilanes." Chemical Science 6, no. 3 (2015): 1735–46. http://dx.doi.org/10.1039/c4sc01592d.
Повний текст джерелаZhou, Xin-Feng, Ya-Dong Wu, Jian-Jun Dai, Yong-Jia Li, Yu Huang, and Hua-Jian Xu. "Borylation of primary and secondary alkyl bromides catalyzed by Cu2O nanoparticles." RSC Advances 5, no. 58 (2015): 46672–76. http://dx.doi.org/10.1039/c5ra06631j.
Повний текст джерелаRueping, Magnus, Shao-Chi Lee, Lin Guo, Huifeng Yue, and Hsuan-Hung Liao. "Nickel-Catalyzed Decarbonylative Silylation, Borylation, and Amination of Arylamides via a Deamidative Reaction Pathway." Synlett 28, no. 19 (October 23, 2017): 2594–98. http://dx.doi.org/10.1055/s-0036-1591495.
Повний текст джерелаHooper, A., A. Zambon, and C. J. Springer. "A novel protocol for the one-pot borylation/Suzuki reaction provides easy access to hinge-binding groups for kinase inhibitors." Organic & Biomolecular Chemistry 14, no. 3 (2016): 963–69. http://dx.doi.org/10.1039/c5ob01915j.
Повний текст джерелаSole, Cristina, Amadeu Bonet, André H. M. de Vries, Johannes G. de Vries, Laurent Lefort, Henrik Gulyás, and Elena Fernández. "Influence of Phosphoramidites in Copper-Catalyzed Conjugate Borylation Reaction." Organometallics 31, no. 22 (April 26, 2012): 7855–61. http://dx.doi.org/10.1021/om300194k.
Повний текст джерелаWelle, Alexandre, Virginie Cirriez, and Olivier Riant. "ChemInform Abstract: Copper Catalyzed Tandem Conjugated Borylation-Aldol Reaction." ChemInform 43, no. 44 (October 4, 2012): no. http://dx.doi.org/10.1002/chin.201244055.
Повний текст джерелаYang, Liting, Jinjin Ma, Xiaomin Peng, Danyang Wang, Tao Guo, Bingxin Yuan, Heng Li, Panke Zhang, and Guanyu Yang. "Rhodium-Catalyzed Borylation/Protonation Tandem Reaction of Hydroxylated Diarylethynes." Asian Journal of Organic Chemistry 6, no. 6 (April 5, 2017): 698–701. http://dx.doi.org/10.1002/ajoc.201700176.
Повний текст джерелаGupta, Shiv S., Krishna K. Sharma, Manoj Prajapati, Gajanan K. Rathod, and Rahul Jain. "Synthesis of Biquinolines via a Pd‐Catalyzed Borylation Reaction." Asian Journal of Organic Chemistry 9, no. 10 (September 6, 2020): 1581–84. http://dx.doi.org/10.1002/ajoc.202000356.
Повний текст джерелаVogels, Christopher M., Paul E. O'Connor, Trevor E. Phillips, Keith J. Watson, Michael P. Shaver, Paul G. Hayes, and Stephen A. Westcott. "Rhodium-catalyzed hydroborations of allylamine and allylimines1." Canadian Journal of Chemistry 79, no. 12 (December 1, 2001): 1898–905. http://dx.doi.org/10.1139/v01-177.
Повний текст джерелаZhu, Jianan, Ying Wei, Dongqing Lin, Changjin Ou, Linghai Xie, Yu Zhao, and Wei Huang. "One-pot synthesis of benzoxaborole derivatives from the palladium-catalyzed cross-coupling reaction of alkoxydiboron with unprotected o-bromobenzylalcohols." Organic & Biomolecular Chemistry 13, no. 46 (2015): 11362–68. http://dx.doi.org/10.1039/c5ob01781e.
Повний текст джерелаIto, Hajime, Eiji Yamamoto, Satoshi Maeda, and Tetsuya Taketsugu. "Transition-Metal-Free Boryl Substitution Using Silylboranes and Alkoxy Bases." Synlett 28, no. 11 (April 26, 2017): 1258–67. http://dx.doi.org/10.1055/s-0036-1588772.
Повний текст джерелаPandarus, Valerica, Geneviève Gingras, François Béland, Rosaria Ciriminna, and Mario Pagliaro. "Clean and fast cross-coupling of aryl halides in one-pot." Beilstein Journal of Organic Chemistry 10 (April 22, 2014): 897–901. http://dx.doi.org/10.3762/bjoc.10.87.
Повний текст джерелаNhari, Laila M., Elham N. Bifari, Aisha R. Al-Marhabi, Huda A. Al-Ghamdi, Sameera N. Al-Ghamdi, Fatimah A. M. Al-Zahrani, Khalid O. Al-Footy, and Reda M. El-Shishtawy. "Synthesis of Novel Key Chromophoric Intermediates via C-C Coupling Reactions." Catalysts 12, no. 10 (October 21, 2022): 1292. http://dx.doi.org/10.3390/catal12101292.
Повний текст джерелаCoffinet, Anaïs, Dan Zhang, Laure Vendier, Sébastien Bontemps, and Antoine Simonneau. "Borane-catalysed dinitrogen borylation by 1,3-B–H bond addition." Dalton Transactions 50, no. 16 (2021): 5582–89. http://dx.doi.org/10.1039/d1dt00317h.
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