Aryl nitrile oxide cycloaddition reactions in the presence of pinacol boronic acid ester

Scholarly Works

• Dresler, E.; Wróblewska, A.; Jasiński, R. Energetic Aspects and Molecular Mechanism of 3-Nitro-substituted 2-Isoxazolines Formation via Nitrile N-Oxide [3+2] Cycloaddition: An MEDT Computational Study. Molecules (Basel, Switzerland) 2024, 29, 3042. doi:10.3390/molecules29133042
• Hernández-Calva, A.; Meléndez-Balbuena, L.; Arroyo-Carranza, M.; Ramírez-Monroy, A. Halogenation of Aldoximes. A Versatile Reaction for the Synthesis of Highly Functionalized Hydroximoyl Chlorides and Furazan N-Oxides. Russian Journal of Organic Chemistry 2023, 59, 2221–2229. doi:10.1134/s1070428023120217
• Chilaka, S. K.; Chellu, R. K.; Soda, A. K.; Kurva, S.; Nanubolu, J. B.; Madabhushi, S. Base‐Catalyzed Domino Reaction Between Aldoxime and N‐Chlorosuccinimide in Alcohol: One‐Pot Synthesis of Alkyl 3‐(3‐Aryl‐1,2,4‐oxadiazol‐5‐yl)propanoates. Advanced Synthesis & Catalysis 2022, 364, 2944–2950. doi:10.1002/adsc.202200265
• Cordero, F. M.; Giomi, D.; Machetti, F. 4.03 – Isoxazoles. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; Vol. 4, pp 308–434. doi:10.1016/b978-0-12-818655-8.00135-9
• Pajkert, R.; Koroniak, H.; Kafarski, P.; Röschenthaler, G.-V. Hypervalent-iodine mediated one-pot synthesis of isoxazolines and isoxazoles bearing a difluoromethyl phosphonate moiety. Organic & biomolecular chemistry 2021, 19, 4871–4876. doi:10.1039/d1ob00685a
• Waheed, M.; Ahmed, N.; Alsharif, M. A.; Alahmdi, M. I.; Mukhtar, S. PhI(OAc)2-Mediated One-Pot Synthesis and their Antibacterial Activity of Flavone and Coumarin Based Isoxazoles Under Mild Reaction Conditions. ChemistrySelect 2019, 4, 1872–1878. doi:10.1002/slct.201803927
• Roscales, S.; Plumet, J. Mini-Review: Organic catalysts in the 1,3-Dipolar cycloaddition reactions of nitrile oxides. HETEROCYCLES 2019, 99, 725. doi:10.3987/rev-18-sr(f)4
• Korgavkar, N. N.; Samant, S. D. 1,3-Dipolar cycloaddition reaction of aryl nitrile oxides with alkenes using imidazole and pyridine containing reusable polymeric base catalysts. Synthetic Communications 2018, 48, 387–394. doi:10.1080/00397911.2017.1399207
• Gioti, E. G.; Koftis, T. V.; Neokosmidis, E.; Vastardi, E.; Kotoulas, S. S.; Trakossas, S.; Tsatsas, T.; Anagnostaki, E. E.; Panagiotidis, T.; Zacharis, C. K.; Tolika, E. P.; Varvogli, A.-A.; Andreou, T.; Gallos, J. K. A new scalable synthesis of entecavir. Tetrahedron 2018, 74, 519–527. doi:10.1016/j.tet.2017.12.034
• Yoshimura, A.; Nguyen, K. C.; Rohde, G. T.; Postnikov, P. S.; Yusubov, M. S.; Zhdankin, V. V. Hypervalent Iodine Reagent Mediated Oxidative Heterocyclization of Aldoximes with Heterocyclic Alkenes. The Journal of organic chemistry 2017, 82, 11742–11751. doi:10.1021/acs.joc.7b01462
• Konnert, L.; Lamaty, F.; Martinez, J.; Colacino, E. Recent Advances in the Synthesis of Hydantoins: The State of the Art of a Valuable Scaffold. Chemical reviews 2017, 117, 13757–13809. doi:10.1021/acs.chemrev.7b00067
• Yoshimura, A.; Nguyen, K. C.; Rohde, G. T.; Saito, A.; Yusubov, M. S.; Zhdankin, V. V. Oxidative Cycloaddition of Aldoximes with Maleimides using Catalytic Hydroxy(aryl)iodonium Species. Advanced Synthesis & Catalysis 2016, 358, 2340–2344. doi:10.1002/adsc.201600331
• Baumann, M.; Baxendale, I. R. The rapid generation of isothiocyanates in flow. Beilstein journal of organic chemistry 2013, 9, 1613–1619. doi:10.3762/bjoc.9.184
• Kumar, K. A.; Govindaraju, M.; Jayaroopa, P.; Kumar, G. V.

Explore citations to this article at