N-acylation of ethanolamine using lipase: a chemoselective catalyst

Scholarly Works

• Sahoo, J.; Panda, J.; Mandal, S.; Sahoo, G. Factors Governing Chemoselectivity in Alkanolamines: A Panoramic Overview. European Journal of Organic Chemistry 2024, 27. doi:10.1002/ejoc.202400160
• Doerr, M.; Romero, A.; Daza, M. C. Effect of the acyl-group length on the chemoselectivity of the lipase-catalyzed acylation of propranolol-a computational study. Journal of molecular modeling 2021, 27, 198. doi:10.1007/s00894-021-04808-y
• Chhatwal, A. R.; Lomax, H. V.; Blacker, A. J.; Williams, J. M. J.; Marcé, P. Direct synthesis of amides from nonactivated carboxylic acids using urea as nitrogen source and Mg(NO3)2 or imidazole as catalysts. Chemical science 2020, 11, 5808–5818. doi:10.1039/d0sc01317j
• Sonawane, R. B.; Sonawane, S. R.; Rasal, N. K.; Jagtap, S. V. Chemoselective O-Formyl and O-Acyl Protection of Alkanolamines, Phenoxyethanols and Alcohols Catalyzed by Nickel-(II) and Copper-(II)-Catalysts. Green Chemistry 2020, 22, 3186–3195. doi:10.1039/d0gc00520g
• Yokoyama, S.; Shibauchi, H.; Asahara, H.; Nishiwaki, N. Metal‐Free O‐Selective Direct Acylation of Amino Alcohols Through Pseudo‐Intramolecular Process. European Journal of Organic Chemistry 2019, 2019, 1125–1133. doi:10.1002/ejoc.201801589
• Piazzolla, F.; Temperini, A. Recent advances in chemoselective acylation of amines. Tetrahedron Letters 2018, 59, 2615–2621. doi:10.1016/j.tetlet.2018.05.065
• Poddar, R.; Jain, A.; Kidwai, M. Bis[(l)prolinate-N,O]Zn: A water-soluble and recycle catalyst for various organic transformations. Journal of advanced research 2017, 8, 245–270. doi:10.1016/j.jare.2016.12.005
• Bergami, M.; Protti, S.; Ravelli, D.; Fagnoni, M. Flow Metal-Free ArC Bond Formation via Photogenerated Phenyl Cations. Advanced Synthesis & Catalysis 2016, 358, 1164–1172. doi:10.1002/adsc.201600019
• Yadav, G. D.; Devendran, S. CHAPTER 4:Microwave Assisted Enzyme Catalysis: Practice and Perspective. White Biotechnology for Sustainable Chemistry; The Royal Society of Chemistry, 2015; pp 52–103. doi:10.1039/9781782624080-00052
• Gelat, F.; Lohier, J.-F.; Gaumont, A.-C.; Perrio, S. tert-Butyl Sulfoxides: Key Precursors for Palladium-Catalyzed Arylation of Sulfenate Salts. Advanced Synthesis & Catalysis 2015, 357, 2011–2016. doi:10.1002/adsc.201500368
• Lundberg, H.; Tinnis, F.; Selander, N.; Adolfsson, H. Catalytic amide formation from non-activated carboxylic acids and amines. Chemical Society reviews 2014, 43, 2714–2742. doi:10.1039/c3cs60345h
• Pavia, C.; Ballerini, E.; Bivona, L. A.; Giacalone, F.; Aprile, C.; Vaccaro, L.; Gruttadauria, M. Palladium Supported on Cross‐Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions. Advanced Synthesis & Catalysis 2013, 355, 2007–2018. doi:10.1002/adsc.201300215
• de M. Muñoz, J.; Alcázar, J.; de la Hoz, A.; Díaz-Ortiz, A. Cross-Coupling in Flow using Supported Catalysts: Mild, Clean, Efficient and Sustainable Suzuki–Miyaura Coupling in a Single Pass. Advanced Synthesis & Catalysis 2012, 354, 3456–3460. doi:10.1002/adsc.201200678
• Kirschning, A.; Kupracz, L.; Hartwig, J. New Synthetic Opportunities in Miniaturized Flow Reactors with Inductive Heating. Chemistry Letters 2012, 41, 562–570. doi:10.1246/cl.2012.562
• Liu, C.; Xiao, S.; Shu, X.; Li, Y.; Xu, L.; Liu, T.; Yu, Y.; Zhang, L.; Liu, H.; Li, Y. Synthesis and photovoltaic properties of novel monoadducts and bisadducts based on amide methanofullerene. ACS applied materials & interfaces 2012, 4, 1065–1071. doi:10.1021/am2016975
• Marrocchi, A.; Tomasi, I.; Vaccaro, L. Organic Small Molecules for Photonics and Electronics from the [2.2]Paracyclophane Scaffold. Israel Journal of Chemistry 2012, 52, 41–52. doi:10.1002/ijch.201100091
• Kidwai, M.; Poddar, R.; Bhardwaj, S. Lipase-catalyzed transformations using poly(ethylene glycol) as solvent. Biocatalysis and Biotransformation 2011, 29, 113–118. doi:10.3109/10242422.2011.578739
• Kidwai, M.; Bhardwaj, S.; Poddar, R. C-Arylation reactions catalyzed by CuO-nanoparticles under ligand free conditions. Beilstein journal of organic chemistry 2010, 6, 35. doi:10.3762/bjoc.6.35
• Poddar, R.

Explore citations to this article at