Asymmetric one-pot sequential Friedel–Crafts-type alkylation and α-oxyamination catalyzed by a peptide and an enzyme

Scholarly Works

• Zhao, H. Recent advances in enzymatic carbon-carbon bond formation. RSC advances 2024, 14, 25932–25974. doi:10.1039/d4ra03885a
• Carceller, J. M.; Arias, K. S.; Climent, M. J.; Iborra, S.; Corma, A. One-pot chemo- and photo-enzymatic linear cascade processes. Chemical Society reviews 2024, 53, 7875–7938. doi:10.1039/d3cs00595j
• Stewart, K. N.; Hawkins, K. G.; Andersen, C. M.; Domaille, D. W. One-pot cascade reactions for the synthesis of dinitroalkanes in aqueous buffer. Reaction Chemistry & Engineering 2023, 8, 1152–1158. doi:10.1039/d2re00403h
• Liu, Y.; Gao, S.; Liu, P.; Kong, W.; Liu, J.; Jiang, Y. Integration of chemo- and bio-catalysis to intensify bioprocesses. Physical Sciences Reviews 2023, 9, 1435–1459. doi:10.1515/psr-2022-0103
• Ascaso‐Alegre, C.; Mangas‐Sanchez, J. Construction of Chemoenzymatic Linear Cascades for the Synthesis of Chiral Compounds. European Journal of Organic Chemistry 2022, 2022. doi:10.1002/ejoc.202200093
• Kudo, K. doi:10.1002/9781119736424.ch5
• doi:10.1002/9783527814268.ch3
• Metrano, A. J.; Chinn, A. J.; Shugrue, C. R.; Stone, E. A.; Kim, B.; Miller, S. J. Asymmetric Catalysis Mediated by Synthetic Peptides, Version 2.0: Expansion of Scope and Mechanisms. Chemical reviews 2020, 120, 11479–11615. doi:10.1021/acs.chemrev.0c00523
• Akagawa, K.; Kudo, K. Design of Peptide Catalysts by Combining Secondary Structural Units for Selective Reactions. Journal of Synthetic Organic Chemistry, Japan 2019, 77, 1222–1233. doi:10.5059/yukigoseikyokaishi.77.1222
• Pauly, J.; Gröger, H.; Patel, A. V. Catalysts Encapsulated in Biopolymer Hydrogels for Chemoenzymatic One‐Pot Processes in Aqueous Media. ChemCatChem 2019, 11, 1503–1509. doi:10.1002/cctc.201802070
• Zhao, Y.-X.; Zhao, Z.-X.; Zhang, H.-X. A DFT study on the mechanism of palladium-catalysed tandem reaction of ortho-electron-deficient alkynyl-substituted aryl aldehydes with indoles. Molecular Physics 2019, 118, e1576933. doi:10.1080/00268976.2019.1576933
• Lachter, E. R.; de A. Rodrigues, J.; Teixeira, V. G.; Mendonça, R. H.; Ribeiro, P. S.; Villabona-Estupiñán, S. Use of Ion-Exchange Resins in Alkylation Reactions. Applications of Ion Exchange Materials in Chemical and Food Industries; Springer International Publishing, 2019; pp 35–74. doi:10.1007/978-3-030-06085-5_3
• Dumeignil, F.; Guehl, M.; Gimbernat, A.; Capron, M.; Ferreira, N. L.; Froidevaux, R.; Girardon, J.-S.; Wojcieszak, R.; Dhulster, P.; Delcroix, D. From sequential chemoenzymatic synthesis to integrated hybrid catalysis: taking the best of both worlds to open up the scope of possibilities for a sustainable future. Catalysis Science & Technology 2018, 8, 5708–5734. doi:10.1039/c8cy01190g
• Pauly, J.; Gröger, H.; Patel, A. V. Metathesis in water conducted by tailor-made encapsulated Grubbs’ catalyst. Green Chemistry 2018, 20, 5179–5187. doi:10.1039/c8gc02164c
• Pauly, J.; Gröger, H.; Patel, A. V. Design, characterisation and application of alginate-based encapsulated pig liver esterase. Journal of biotechnology 2018, 280, 42–48. doi:10.1016/j.jbiotec.2018.05.017
• Szőllősi, G. Asymmetric one-pot reactions using heterogeneous chemical catalysis: recent steps towards sustainable processes. Catalysis Science & Technology 2018, 8, 389–422. doi:10.1039/c7cy01671a
• Akagawa, K. 19 – Catalysis by peptides. Peptide Applications in Biomedicine, Biotechnology and Bioengineering; Elsevier, 2018; pp 513–564. doi:10.1016/b978-0-08-100736-5.00021-1
• Bisogno, F. R.; López-Vidal, M. G.; de Gonzalo, G. Organocatalysis and Biocatalysis Hand in Hand: Combining Catalysts in One‐Pot Procedures. Advanced Synthesis & Catalysis 2017, 359, 2026–2049. doi:10.1002/adsc.201700158
• Schrittwieser, J. H.; Velikogne, S.; Hall, M.; Kroutil, W. Artificial Biocatalytic Linear Cascades for Preparation of Organic Molecules. Chemical reviews 2017, 118, 270–348. doi:10.1021/acs.chemrev.7b00033
• Xue, J.-W.; Guo, J.-T.; He, Y.-H.; Guan, Z. Solvent-Controlled Enzyme-Catalyzed Friedel-Crafts Reactions of Indoles and Isatins by Using α-Chymotrypsin. Asian Journal of Organic Chemistry 2017, 6, 297–304. doi:10.1002/ajoc.201600526

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