Reductive amination with zinc powder in aqueous media

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• Wang, T.; Wu, M.; Qiu, S.; Ming, H.; Yuan, Y.; Liu, M.; Yue, J.; Huang, F. Borane as reducing reagent of nitroarenes. Tetrahedron 2024, 151, 133790. doi:10.1016/j.tet.2023.133790
• Jiang, H.; Wu, X.; Zhang, H.; Yan, Q.; Li, H.; Ma, T.; Yang, S. Toward effective electrocatalytic C–N coupling for the synthesis of organic nitrogenous compounds using CO2 and biomass as carbon sources. SusMat 2023, 3, 781–820. doi:10.1002/sus2.175
• Surman, M. D.; Chen, P.; Avramovitch, B.; Haber, K.; Buckle, R. N.; Gazal, S. Preparation of Sitagliptin M2 and M5 metabolites and degradation impurities through a stereocontrolled amidine reduction. Tetrahedron Letters 2022, 106, 154058. doi:10.1016/j.tetlet.2022.154058
• Kawahara, N.; Palasin, K.; Asano, Y. Novel Enzymatic Method for Imine Synthesis via the Oxidation of Primary Amines Using D-Amino Acid Oxidase from Porcine Kidney. Catalysts 2022, 12, 511. doi:10.3390/catal12050511
• Kim, J. E.; Jang, J. H.; Lee, K. M.; Balamurugan, M.; Jo, Y. I.; Lee, M. Y.; Choi, S.; Im, S. W.; Nam, K. T. Electrochemical Synthesis of Glycine from Oxalic Acid and Nitrate. Angewandte Chemie (International ed. in English) 2021, 60, 21943–21951. doi:10.1002/anie.202108352
• Kim, J. E.; Jang, J. H.; Lee, K. M.; Balamurugan, M.; Jo, Y. I.; Lee, M. Y.; Choi, S.; Im, S. W.; Nam, K. T. Electrochemical Synthesis of Glycine from Oxalic Acid and Nitrate. Angewandte Chemie 2021, 133, 22114–22122. doi:10.1002/ange.202108352
• Liu, J.; Song, Y.; Ma, L. Earth-abundant Metal-catalyzed Reductive Amination: Recent Advances and Prospect for Future Catalysis. Chemistry, an Asian journal 2021, 16, 2371–2391. doi:10.1002/asia.202100473
• Ruscoe, R. E.; Ramsden, J. I.; Turner, N. J. Redox surrogate methods for sustainable amine N-alkylation. Current Opinion in Chemical Engineering 2020, 30, 60–68. doi:10.1016/j.coche.2020.08.005
• Nori, V.; Dasgupta, A.; Babaahmadi, R.; Carlone, A.; Ariafard, A.; Melen, R. L. Triarylborane catalysed N-alkylation of amines with aryl esters. Catalysis Science & Technology 2020, 10, 7523–7530. doi:10.1039/d0cy01339k
• Kim, J. E.; Choi, S.; Balamurugan, M.; Jang, J. H.; Nam, K. T. Electrochemical C–N Bond Formation for Sustainable Amine Synthesis. Trends in Chemistry 2020, 2, 1004–1019. doi:10.1016/j.trechm.2020.09.003
• Thepmanee, O.; Prapainop, K.; Noppha, O.; Rattanawimanwong, N.; Siangproh, W.; Chailapakul, O.; Songsrirote, K. A simple paper-based approach for arsenic determination in water using hydride generation coupled with mercaptosuccinic-acid capped CdTe quantum dots. Analytical methods : advancing methods and applications 2020, 12, 2718–2726. doi:10.1039/d0ay00273a
• Ando, S.; Ishizuka, T. Diastereoselective Reductions with Zinc Powder in a Mixture of NaOH aq. and MeOH for Syntheses of (±)-1,2-Diarylethylenediamines. Advanced Synthesis & Catalysis 2018, 360, 4820–4826. doi:10.1002/adsc.201800976
• Porras, A. M. G.; Terra, B. S.; Braga, T. C.; Magalhães, T. F. F.; Martins, C. V. B.; da Silva, D. L.; Baltazar, L. M.; Gouveia, L. F.; de Freitas, G. J. C.; Santos, D. A.; Resende-Stoianoff, M. A.; Fuchs, B. B.; Mylonakis, E.; de Freitas, R. P.; de Fátima, Â. Butenafine and analogues: An expeditious synthesis and cytotoxicity and antifungal activities. Journal of advanced research 2018, 14, 81–91. doi:10.1016/j.jare.2018.06.004
• Mondal, K.; Pan, S. C. Organocatalytic Asymmetric Domino Michael/Acyl Transfer Reaction between γ/δ-Hydroxyenones and α-Nitroketones. The Journal of organic chemistry 2018, 83, 5301–5312. doi:10.1021/acs.joc.8b00436
• Arrabito, G.; Errico, V.; Zhang, Z.; Han, W.; Falconi, C. Nanotransducers on printed circuit boards by rational design of high-density, long, thin and untapered ZnO nanowires. Nano Energy 2018, 46, 54–62. doi:10.1016/j.nanoen.2018.01.029
• Roylance, J. J.; Choi, K.-S. Electrochemical reductive amination of furfural-based biomass intermediates. Green Chemistry 2016, 18, 5412–5417. doi:10.1039/c6gc01541g
• Zhu, M. Transfer hydrogenative reductive amination of aldehydes in aqueous sodium formate solution. Tetrahedron Letters 2016, 57, 509–511. doi:10.1016/j.tetlet.2015.12.072
• Gusak, K. N.; Ignatovich, Z. V.; Koroleva, E. V. New potential of the reductive alkylation of amines. Russian Chemical Reviews 2015, 84, 288–309. doi:10.1070/rcr4443
• Howard, J. K.; Hyland, C. J. T. Synthetic methods Part (ii) oxidation and reduction methods. Natural Product Reports 2012, 108, 29–52.
• Mitkina, T.; Stanglmair, C.; Setzer, W.; Gruber, M.; Kisch, H.; König, B. Visible light mediated homo- and heterocoupling of benzyl alcohols and benzyl amines on polycrystalline cadmium sulfide. Organic & biomolecular chemistry 2012, 10, 3556–3561. doi:10.1039/c2ob07053g

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