Artículos de revistas sobre el tema "Alkyl-Aryl couplings"
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Bisz, Elwira y Michal Szostak. "Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Aryl Chlorobenzoates with Alkyl Grignard Reagents". Molecules 25, n.º 1 (6 de enero de 2020): 230. http://dx.doi.org/10.3390/molecules25010230.
Texto completoXu, Meng-Yu y Bin Xiao. "Germatranes and carbagermatranes: (hetero)aryl and alkyl coupling partners in Pd-catalyzed cross-coupling reactions". Chemical Communications 57, n.º 89 (2021): 11764–75. http://dx.doi.org/10.1039/d1cc04373k.
Texto completoBernauer, Josef, Guojiao Wu y Axel Jacobi von Wangelin. "Iron-catalysed allylation–hydrogenation sequences as masked alkyl–alkyl cross-couplings". RSC Advances 9, n.º 54 (2019): 31217–23. http://dx.doi.org/10.1039/c9ra07604b.
Texto completoCrisp, GT y S. Papadopoulos. "Palladium-Mediated Transformations of Heteroaromatic Triflates". Australian Journal of Chemistry 42, n.º 2 (1989): 279. http://dx.doi.org/10.1071/ch9890279.
Texto completoCauley, Anthony N., Melda Sezen-Edmonds, Eric M. Simmons y Cullen L. Cavallaro. "Increasing saturation: development of broadly applicable photocatalytic Csp2–Csp3 cross-couplings of alkyl trifluoroborates and (hetero)aryl bromides for array synthesis". Reaction Chemistry & Engineering 6, n.º 9 (2021): 1666–76. http://dx.doi.org/10.1039/d1re00192b.
Texto completoDavis, Mia, Mathias O. Senge y Oliver B. Locos. "Anthracenylporphyrins". Zeitschrift für Naturforschung B 65, n.º 12 (1 de diciembre de 2010): 1472–84. http://dx.doi.org/10.1515/znb-2010-1211.
Texto completoParmar, Dixit, Lena Henkel, Josef Dib y Magnus Rueping. "Iron catalysed cross-couplings of azetidines – application to the formal synthesis of a pharmacologically active molecule". Chemical Communications 51, n.º 11 (2015): 2111–13. http://dx.doi.org/10.1039/c4cc09337b.
Texto completoPaul, Avishek, Mark D. Smith y Aaron K. Vannucci. "Photoredox-Assisted Reductive Cross-Coupling: Mechanistic Insight into Catalytic Aryl–Alkyl Cross-Couplings". Journal of Organic Chemistry 82, n.º 4 (2 de febrero de 2017): 1996–2003. http://dx.doi.org/10.1021/acs.joc.6b02830.
Texto completoVillanueva-Kasis, Oscar, Denisse A. de Loera, Sandra L. Castañón-Alonso, Armando Domínguez-Ortiz, Leticia Lomas-Romero, Ilich A. Ibarra, Eduardo González-Zamora y Alejandro Islas-Jácome. "Efficient Synthesis of New α-β-Unsaturated Alkyl-Ester Peptide-Linked Chiral Amines". Proceedings 9, n.º 1 (14 de noviembre de 2018): 34. http://dx.doi.org/10.3390/ecsoc-22-05769.
Texto completoSedláček, Ondřej, Petra Břehová, Radek Pohl, Antonín Holý y Zlatko Janeba. "The synthesis of the 8-C-substituted 2,6-diamino-9-[2-(phosphonomethoxy)ethyl]purine (PMEDAP) derivatives by diverse cross-coupling reactions". Canadian Journal of Chemistry 89, n.º 4 (abril de 2011): 488–98. http://dx.doi.org/10.1139/v11-001.
Texto completoCornella, Josep y Matthew O’Neill. "Retaining Alkyl Nucleophile Regiofidelity in Transition-Metal-Mediated Cross-Couplings to Aryl Electrophiles". Synthesis 50, n.º 20 (10 de septiembre de 2018): 3974–96. http://dx.doi.org/10.1055/s-0037-1609941.
Texto completoLiu, Lei, Maria Camila Aguilera, Wes Lee, Cassandra R. Youshaw, Michael L. Neidig y Osvaldo Gutierrez. "General method for iron-catalyzed multicomponent radical cascades–cross-couplings". Science 374, n.º 6566 (22 de octubre de 2021): 432–39. http://dx.doi.org/10.1126/science.abj6005.
Texto completoPerkins, Robert J., Alexander J. Hughes, Daniel J. Weix y Eric C. Hansen. "Metal-Reductant-Free Electrochemical Nickel-Catalyzed Couplings of Aryl and Alkyl Bromides in Acetonitrile". Organic Process Research & Development 23, n.º 8 (22 de julio de 2019): 1746–51. http://dx.doi.org/10.1021/acs.oprd.9b00232.
Texto completoPang, Haobo, Ye Wang, Fabrice Gallou y Bruce H. Lipshutz. "Fe-Catalyzed Reductive Couplings of Terminal (Hetero)Aryl Alkenes and Alkyl Halides under Aqueous Micellar Conditions". Journal of the American Chemical Society 141, n.º 43 (27 de septiembre de 2019): 17117–24. http://dx.doi.org/10.1021/jacs.9b04510.
Texto completoAlsabeh, Pamela G. y Mark Stradiotto. "Addressing Challenges in Palladium-Catalyzed Cross-Couplings of Aryl Mesylates: Monoarylation of Ketones and Primary Alkyl Amines". Angewandte Chemie 125, n.º 28 (12 de junio de 2013): 7383–87. http://dx.doi.org/10.1002/ange.201303305.
Texto completoAlsabeh, Pamela G. y Mark Stradiotto. "Addressing Challenges in Palladium-Catalyzed Cross-Couplings of Aryl Mesylates: Monoarylation of Ketones and Primary Alkyl Amines". Angewandte Chemie International Edition 52, n.º 28 (12 de junio de 2013): 7242–46. http://dx.doi.org/10.1002/anie.201303305.
Texto completoShen, Zhi-Liang, Kelvin Kau Kiat Goh, Yong-Sheng Yang, Yin-Chang Lai, Colin Hong An Wong, Hao-Lun Cheong y Teck-Peng Loh. "Direct Synthesis of Water-Tolerant Alkyl Indium Reagents and Their Application in Palladium-Catalyzed Couplings with Aryl Halides". Angewandte Chemie International Edition 50, n.º 2 (5 de diciembre de 2010): 511–14. http://dx.doi.org/10.1002/anie.201005798.
Texto completoShen, Zhi-Liang, Kelvin Kau Kiat Goh, Yong-Sheng Yang, Yin-Chang Lai, Colin Hong An Wong, Hao-Lun Cheong y Teck-Peng Loh. "Direct Synthesis of Water-Tolerant Alkyl Indium Reagents and Their Application in Palladium-Catalyzed Couplings with Aryl Halides". Angewandte Chemie 123, n.º 2 (5 de diciembre de 2010): 531–34. http://dx.doi.org/10.1002/ange.201005798.
Texto completoAlsabeh, Pamela G. y Mark Stradiotto. "ChemInform Abstract: Addressing Challenges in Palladium-Catalyzed Cross-Couplings of Aryl Mesylates: Monoarylation of Ketones and Primary Alkyl Amines." ChemInform 44, n.º 48 (8 de noviembre de 2013): no. http://dx.doi.org/10.1002/chin.201348089.
Texto completoShen, Zhi-Liang, Kelvin Kau Kiat Goh, Yong-Sheng Yang, Yin-Chang Lai, Colin Hong An Wong, Hao-Lun Cheong y Teck-Peng Loh. "ChemInform Abstract: Direct Synthesis of Water-Tolerant Alkyl Indium Reagents and Their Application in Palladium-Catalyzed Couplings with Aryl Halides." ChemInform 42, n.º 20 (21 de abril de 2011): no. http://dx.doi.org/10.1002/chin.201120040.
Texto completoLi, Zhuang, Bing Lu, Hongmei Sun, Qi Shen y Yong Zhang. "Ionic iron(III) complexes bearing a dialkylbenzimidazolium cation: Efficient catalysts for magnesium-mediated cross-couplings of aryl phosphates with alkyl bromides". Applied Organometallic Chemistry 31, n.º 8 (12 de diciembre de 2016): e3671. http://dx.doi.org/10.1002/aoc.3671.
Texto completoMa, Dawei y Jiqing Jiang. "Pd/Cu-catalyzed couplings of β-amino esters with aryl bromides. Synthesis of chiral 1,2,3,4-tetrahydro-4-oxo-2-alkyl-1-quinolines". Tetrahedron: Asymmetry 9, n.º 7 (abril de 1998): 1137–42. http://dx.doi.org/10.1016/s0957-4166(98)00078-0.
Texto completoMA, D. y J. JIANG. "ChemInform Abstract: Pd/Cu-Catalyzed Couplings of β-Amino Esters with Aryl Bromides. Synthesis of Chiral 1,2,3,4-Tetrahydro-4-oxo-2-alkyl-1-quinolines." ChemInform 29, n.º 34 (20 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199834171.
Texto completoYuan, Mingbin, Zhihui Song, Shorouk O. Badir, Gary A. Molander y Osvaldo Gutierrez. "On the Nature of C(sp3)–C(sp2) Bond Formation in Nickel-Catalyzed Tertiary Radical Cross-Couplings: A Case Study of Ni/Photoredox Catalytic Cross-Coupling of Alkyl Radicals and Aryl Halides". Journal of the American Chemical Society 142, n.º 15 (20 de marzo de 2020): 7225–34. http://dx.doi.org/10.1021/jacs.0c02355.
Texto completoYuan, Jiwen, Chao Liu y Aiwen Lei. "Oxidative cross S–H/S–H coupling: selective synthesis of unsymmetrical aryl tert-alkyl disulfanes". Organic Chemistry Frontiers 2, n.º 6 (2015): 677–80. http://dx.doi.org/10.1039/c5qo00027k.
Texto completoJia, Xiao, Xinghua Zhang, Qun Qian y Hegui Gong. "Alkyl–aryl ketone synthesis via nickel-catalyzed reductive coupling of alkyl halides with aryl acids and anhydrides". Chemical Communications 51, n.º 51 (2015): 10302–5. http://dx.doi.org/10.1039/c5cc03113c.
Texto completoDey, Supriya y Narayanaswamy Jayaraman. "Branching out at C-2 of septanosides. Synthesis of 2-deoxy-2-C-alkyl/aryl septanosides from a bromo-oxepine". Beilstein Journal of Organic Chemistry 8 (10 de abril de 2012): 522–27. http://dx.doi.org/10.3762/bjoc.8.59.
Texto completoSakai, Norio, Hiromu Maeda y Yohei Ogiwara. "Copper-Catalyzed Three-Component Coupling Reaction of Aryl Iodides, a Disilathiane, and Alkyl Benzoates Leading to a One-Pot Synthesis of Alkyl Aryl Sulfides". Synthesis 51, n.º 11 (18 de marzo de 2019): 2323–30. http://dx.doi.org/10.1055/s-0037-1610869.
Texto completoKumaraswamy, Gullapalli, Ragam Raju y Vykunthapu Narayanarao. "Metal- and base-free syntheses of aryl/alkylthioindoles by the iodine-induced reductive coupling of aryl/alkyl sulfonyl chlorides with indoles". RSC Advances 5, n.º 29 (2015): 22718–23. http://dx.doi.org/10.1039/c5ra00646e.
Texto completoLi, Chengxi, Guolan Xiao, Qing Zhao, Huimin Liu, Tao Wang y Wenjun Tang. "Sterically demanding aryl–alkyl Suzuki–Miyaura coupling". Org. Chem. Front. 1, n.º 3 (2014): 225–29. http://dx.doi.org/10.1039/c4qo00024b.
Texto completoBisz, Elwira. "Iron-Catalyzed Cross-Coupling Reactions of Alkyl Grignards with Aryl Chlorobenzenesulfonates". Molecules 26, n.º 19 (29 de septiembre de 2021): 5895. http://dx.doi.org/10.3390/molecules26195895.
Texto completoZhu, Dan y Lei Shi. "Ni-Catalyzed cross-coupling of aryl thioethers with alkyl Grignard reagents via C–S bond cleavage". Chemical Communications 54, n.º 67 (2018): 9313–16. http://dx.doi.org/10.1039/c8cc03665a.
Texto completoAtar, Amol Balu, Jongmin Kang y Arvind H. Jadhav. "A [bmim]Cl-promoted domino protocol using an isocyanide-based [4+1]-cycloaddition reaction for the synthesis of diversely functionalized 3-alkylamino-2-alkyl/aryl/hetero-aryl indolizine-1-carbonitriles under solvent-free conditions". New Journal of Chemistry 44, n.º 8 (2020): 3241–48. http://dx.doi.org/10.1039/c9nj05738b.
Texto completoSang, Dayong, Jiahui Wang, Yun Zheng, Jianyuan He, Caili Yuan, Qing An y Juan Tian. "Carbodiimides as Acid Scavengers in Aluminum Triiodide Induced Cleavage of Alkyl Aryl Ethers". Synthesis 49, n.º 12 (14 de marzo de 2017): 2721–26. http://dx.doi.org/10.1055/s-0036-1588755.
Texto completoZhu, Jiayi, Yu Chen, Feng Lin, Baoshuang Wang, Zhengwang Chen y Liangxian Liu. "NiSO4-catalyzed C–H activation/C–S cross-coupling of 1,2,3-triazole N-oxides with thiols". Organic & Biomolecular Chemistry 13, n.º 12 (2015): 3711–20. http://dx.doi.org/10.1039/c4ob02586e.
Texto completoSingh, Pratibha, Rekha Bai, Rakhee Choudhary, Mahesh C. Sharma y Satpal Singh Badsara. "Regio- and stereoselective syntheses of allylic thioethers under metal free conditions". RSC Advances 7, n.º 49 (2017): 30594–602. http://dx.doi.org/10.1039/c7ra04817c.
Texto completoWang, Dungai, Jinlong Zhao, Weigang Xu, Changwei Shao, Zheng Shi, Liang Li y Xinghua Zhang. "Metal- and base-free reductive coupling reaction of P(O)–H with aryl/alkyl sulfonyl chlorides: a novel protocol for the construction of P–S–C bonds". Organic & Biomolecular Chemistry 15, n.º 3 (2017): 545–49. http://dx.doi.org/10.1039/c6ob02364a.
Texto completoLi, Zhuang, Ling Liu, Hong-mei Sun, Qi Shen y Yong Zhang. "Alkyl Grignard cross-coupling of aryl phosphates catalyzed by new, highly active ionic iron(ii) complexes containing a phosphine ligand and an imidazolium cation". Dalton Transactions 45, n.º 44 (2016): 17739–47. http://dx.doi.org/10.1039/c6dt02995g.
Texto completoLin, Yang, Mingzhong Cai, Zhiqiang Fang y Hong Zhao. "MCM-41-immobilized 1,10-phenanthroline–copper(i) complex: a highly efficient and recyclable catalyst for the coupling of aryl iodides with aliphatic alcohols". RSC Advances 6, n.º 88 (2016): 85186–93. http://dx.doi.org/10.1039/c6ra19825b.
Texto completoWang, Junlei, Binbin Huang, Chao Yang y Wujiong Xia. "Visible-light-mediated defluorinative cross-coupling of gem-difluoroalkenes with thiols". Chemical Communications 55, n.º 74 (2019): 11103–6. http://dx.doi.org/10.1039/c9cc05293c.
Texto completoMukai, Shoma y Nathan Werner. "Synthesis and Palladium-Catalyzed Cross-Coupling of an Alkyl-Substituted Alkenylboronic Acid Pinacol Ester with Aryl Bromides". American Journal of Undergraduate Research 20, n.º 1 (30 de junio de 2023): 37–46. http://dx.doi.org/10.33697/ajur.2023.078.
Texto completoRoslin, Sara y Luke R. Odell. "Palladium and visible-light mediated carbonylative Suzuki–Miyaura coupling of unactivated alkyl halides and aryl boronic acids". Chemical Communications 53, n.º 51 (2017): 6895–98. http://dx.doi.org/10.1039/c7cc02763j.
Texto completoReddy, P. Linga, R. Arundhathi y Diwan S. Rawat. "Cu(0)@Al2O3/SiO2 NPs: an efficient reusable catalyst for the cross coupling reactions of aryl chlorides with amines and anilines". RSC Advances 5, n.º 112 (2015): 92121–27. http://dx.doi.org/10.1039/c5ra19337k.
Texto completoWang, Xie, Peipei Xie, Renhua Qiu, Longzhi Zhu, Ting Liu, You Li, Takanori Iwasaki et al. "Nickel-catalysed direct alkylation of thiophenes via double C(sp3)–H/C(sp2)–H bond cleavage: the importance of KH2PO4". Chemical Communications 53, n.º 59 (2017): 8316–19. http://dx.doi.org/10.1039/c7cc04252c.
Texto completoCarrasco, Desirée, Mónica H. Pérez-Temprano, Juan A. Casares y Pablo Espinet. "Cross Alkyl–Aryl versus Homo Aryl–Aryl Coupling in Palladium-Catalyzed Coupling of Alkyl–Gold(I) and Aryl–Halide". Organometallics 33, n.º 13 (24 de junio de 2014): 3540–45. http://dx.doi.org/10.1021/om500446x.
Texto completoSumida, Yuto, Takamitsu Hosoya y Tomoe Sumida. "Nickel-Catalyzed Reductive Cross-Coupling of Aryl Triflates and Nonaflates with Alkyl Iodides". Synthesis 49, n.º 16 (28 de junio de 2017): 3590–601. http://dx.doi.org/10.1055/s-0036-1588464.
Texto completoWu, Sisi, Weijia Shi y Gang Zou. "Mechanical metal activation for Ni-catalyzed, Mn-mediated cross-electrophile coupling between aryl and alkyl bromides". New Journal of Chemistry 45, n.º 25 (2021): 11269–74. http://dx.doi.org/10.1039/d1nj01732b.
Texto completoLi, Wei-Ze y Zhong-Xia Wang. "A nickel-catalyzed silylation reaction of alkyl aryl sulfoxides with silylzinc reagents". Organic & Biomolecular Chemistry 19, n.º 23 (2021): 5082–86. http://dx.doi.org/10.1039/d1ob00840d.
Texto completoLévêque, Christophe, Ludwig Chenneberg, Vincent Corcé, Jean-Philippe Goddard, Cyril Ollivier y Louis Fensterbank. "Primary alkyl bis-catecholato silicates in dual photoredox/nickel catalysis: aryl- and heteroaryl-alkyl cross coupling reactions". Organic Chemistry Frontiers 3, n.º 4 (2016): 462–65. http://dx.doi.org/10.1039/c6qo00014b.
Texto completoSong, Liu-Yi, Meng-Ke Chen, Jian Wang y Jing-Hua Li. "A straightforward coupling of 4-sulfonylpyridines with Grignard reagents". Journal of Chemical Research 46, n.º 3 (marzo de 2022): 174751982211035. http://dx.doi.org/10.1177/17475198221103502.
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