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