C–C Bond formation catalyzed by natural gelatin and collagen proteins

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• Zhao, H. Recent advances in enzymatic carbon-carbon bond formation. RSC advances 2024, 14, 25932–25974. doi:10.1039/d4ra03885a
• Wang, L.; Zhang, M.; Teng, H.; Wang, Z.; Wang, S.; Li, P.; Wu, J.; Yang, L.; Xu, G. Rationally introducing non-canonical amino acids to enhance catalytic activity of LmrR for Henry reaction. Bioresources and bioprocessing 2024, 11, 26. doi:10.1186/s40643-024-00744-w
• Saavedra, B.; Meli, A.; Rizzo, C.; Ramón, D. J.; D'Anna, F. Natural eutectogels: sustainable catalytic systems for C–C bond formation reactions. Green Chemistry 2021, 23, 6555–6565. doi:10.1039/d1gc01647d
• Kowalczyk, D.; Skrzypek, T.; Basiura-Cembala, M.; Łupina, K.; Mężyńska, M. The effect of potassium sorbate on the physicochemical properties of edible films based on pullulan, gelatin and their blends. Food Hydrocolloids 2020, 105, 105837. doi:10.1016/j.foodhyd.2020.105837
• Meninno, S. Valorization of Waste: Sustainable Organocatalysts from Renewable Resources. ChemSusChem 2019, 13, 439–468. doi:10.1002/cssc.201902500
• Khoury, C.; Pappuru, S.; Gavriely, N.; Kleinerman, O.; Shpasser, D.; Segal-Peretz, T.; Gazit, O. M. Cooperatively Catalyzed Henry Reaction through Directed Metal‐Chitosan Interactions. ChemNanoMat 2019, 5, 1498–1505. doi:10.1002/cnma.201900431
• Xu, C.; Nasrollahzadeh, M.; Sajjadi, M.; Maham, M.; Luque, R.; Puente-Santiago, A. R. Benign-by-design nature-inspired nanosystems in biofuels production and catalytic applications. Renewable and Sustainable Energy Reviews 2019, 112, 195–252. doi:10.1016/j.rser.2019.03.062
• Smitha, G.; Sreekumar, K.; Elsymol, G.; Sudhishna, P. Synthesis of heterogeneous catalysts and study of its catalytic activity towards Henry reaction and Asymmetric aldol reaction. Materials Today: Proceedings 2019, 9, 46–53. doi:10.1016/j.matpr.2019.02.035
• Wang, L.; Hou, Y.; Zhong, X.; Hu, J.; Shi, F.; Mi, H. Preparation and catalytic performance of alginate-based Schiff Base. Carbohydrate polymers 2018, 208, 42–49. doi:10.1016/j.carbpol.2018.12.062
• Häring, M.; Tautz, M.; Alegre-Requena, J. V.; Saldías, C.; Díaz, D. D. Non-enzyme entrapping biohydrogels in catalysis. Tetrahedron Letters 2018, 59, 3293–3306. doi:10.1016/j.tetlet.2018.07.029
• Kumar, N. S.; Bheeram, V. R.; Mukkamala, S. B.; Rao, L. C.; Vasantha, R. An Efficient and Environmentally Benign Protocol for the 1,6-Michael Addition of Nitroalkanes to 3-Methyl-4-nitro-5-styrylisoxazoles in WERSA. ChemistrySelect 2018, 3, 1915–1918. doi:10.1002/slct.201702788
• Liu, X.; Manzur, C.; Novoa, N.; Celedón, S.; Carrillo, D.; Hamon, J.-R. Multidentate unsymmetrically-substituted Schiff bases and their metal complexes: Synthesis, functional materials properties, and applications to catalysis. Coordination Chemistry Reviews 2018, 357, 144–172. doi:10.1016/j.ccr.2017.11.030
• Kumari, S.; Häring, M.; Gupta, S. S.; Díaz, D. D. Catalytic Macroporous Biohydrogels Made of Ferritin-Encapsulated Gold Nanoparticles. ChemPlusChem 2016, 82, 225–232. doi:10.1002/cplu.201600454
• Häring, M.; Pettignano, A.; Quignard, F.; Tanchoux, N.; Díaz, D. D. Keratin Protein-Catalyzed Nitroaldol (Henry) Reaction and Comparison with Other Biopolymers. Molecules (Basel, Switzerland) 2016, 21, 1122. doi:10.3390/molecules21091122
• Mekhail, G. M.; Kamel, A. O.; Awad, G. A.; Mortada, N. D.; Rodrigo, R. L.; Spagnuolo, P. A.; Wettig, S. D. Synthesis and evaluation of alendronate-modified gelatin biopolymer as a novel osteotropic nanocarrier for gene therapy. Nanomedicine (London, England) 2016, 11, 2251–2273. doi:10.2217/nnm-2016-0151
• Häring, M.; Pérez-Madrigal, M. M.; Kühbeck, D.; Pettignano, A.; Quignard, F.; Díaz, D. D. DNA-catalyzed Henry reaction in pure water and the striking influence of organic buffer systems. Molecules (Basel, Switzerland) 2015, 20, 4136–4147. doi:10.3390/molecules20034136
• Miao, Y.; Rahimi, M.; Geertsema, E. M.; Poelarends, G. J. Recent developments in enzyme promiscuity for carbon-carbon bond-forming reactions. Current opinion in chemical biology 2015, 25, 115–123. doi:10.1016/j.cbpa.2014.12.020
• Kühbeck, D.; Mayr, J.; Häring, M.; Hofmann, M.; Quignard, F.; Díaz, D. D. Evaluation of the nitroaldol reaction in the presence of metal ion-crosslinked alginates. New Journal of Chemistry 2015, 39, 2306–2315. doi:10.1039/c4nj02178a
• Palmieri, A.; Gabrielli, S.; Sampaolesi, S.; Ballini, R. Nitroaldol (Henry) reaction of 2-oxoaldehydes with nitroalkanes as a strategic step for a useful, one-pot synthesis of 1,2-diketones. RSC Advances 2015, 5, 36652–36655. doi:10.1039/c5ra03772g
• Pettignano, A.; Bernardi, L.; Fochi, M.; Geraci, L.; Robitzer, M.; Tanchoux, N.; Quignard, F. Alginic acid aerogel: a heterogeneous Brønsted acid promoter for the direct Mannich reaction. New Journal of Chemistry 2015, 39, 4222–4226. doi:10.1039/c5nj00349k

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