α-Bromodiazoacetamides – a new class of diazo compounds for catalyst-free, ambient temperature intramolecular C–H insertion reactions

Scholarly Works

• Wright, B. A.; Regni, A.; Chaisan, N.; Sarpong, R. Navigating Excess Complexity: Total Synthesis of Daphenylline. Journal of the American Chemical Society 2024, 146, 1813–1818. doi:10.1021/jacs.3c12953
• Váradi, B.; Brezovcsik, K.; Garda, Z.; Madarasi, E.; Szedlacsek, H.; Badea, R.-A.; Vasilescu, A.-M.; Puiu, A.-G.; Ionescu, A. E.; Sima, L.-E.; Munteanu, C. V. A.; Călăraş, S.; Vágner, A.; Szikra, D.; Toàn, N. M.; Nagy, T.; Szűcs, Z.; Szedlacsek, S.; Nagy, G.; Tircsó, G. Synthesis and characterization of a novel [52Mn]Mn-labelled affibody based radiotracer for HER2+ targeting. Inorganic Chemistry Frontiers 2023, 10, 4734–4745. doi:10.1039/d3qi00356f
• Yi, Y.; Zhang, J.; Zuo, J.; Zhang, M.; Yang, S.; Huang, Z.; Li, G.; Shang, R.; Lin, S. Novel pyridinium cationic pleuromutilin analogues overcoming bacterial multidrug resistance. European journal of medicinal chemistry 2023, 251, 115269. doi:10.1016/j.ejmech.2023.115269
• Lagoutte, R.; Lefebvre, Q.; Salomé, C.; Fessard, T. Comprehensive Heterocyclic Chemistry IV - Other Fused Azetidines, Azetines and Azetes. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 159–211. doi:10.1016/b978-0-12-818655-8.00161-x
• Boni, Y. T.; Wei, B.; Davies, H. M. L. Synthetic Applications of Carbene and Nitrene C H Insertion. Comprehensive Organometallic Chemistry IV; Elsevier, 2022; pp 251–293. doi:10.1016/b978-0-12-820206-7.00157-8
• Kálmán, F. K.; Nagy, V.; Uzal-Varela, R.; Pérez-Lourido, P.; Esteban-Gómez, D.; Garda, Z.; Pota, K.; Mezei, R.; Pallier, A.; Tóth, É.; Platas-Iglesias, C.; Tircsó, G. Expanding the Ligand Classes Used for Mn(II) Complexation: Oxa-aza Macrocycles Make the Difference. Molecules (Basel, Switzerland) 2021, 26, 1524. doi:10.3390/molecules26061524
• Atsushi, T.; Yukiko, K.; Kazuyuki, S.; Kentaro, K.; Masaaki, O. Stereoselective Synthesis of Multisubstituted α-fluoro-β-lactams. Current Organic Chemistry 2020, 24, 2169–2180. doi:10.2174/1385272824666200221114707
• Fujii, T.; Thu, H. D. T.; Iwasa, S. Synthesis of γ-lactams via Ru(II)–Pheox-catalyzed regioselective intramolecular Csp3–H insertion of diazoacetamides. Tetrahedron Letters 2020, 61, 152276. doi:10.1016/j.tetlet.2020.152276
• Jain, B.; Negi, R.; Singh, A. K. Oxidative behavior of N -bromophthalimide for organic compounds: a review. SN Applied Sciences 2018, 1, 1–11. doi:10.1007/s42452-018-0100-1
• Garda, Z.; Molnár, E.; Kálmán, F. K.; Botár, R.; Nagy, V.; Baranyai, Z.; Brücher, E.; Kovacs, Z.; Tóth, I.; Tircsó, G. Effect of the nature of donor atoms on the thermodynamic, kinetic and relaxation properties of Mn(II) complexes formed with some trisubstituted 12 membered macrocyclic ligands. Frontiers in chemistry 2018, 6, 232. doi:10.3389/fchem.2018.00232
• Burtoloso, A. C. B.; Momo, P. B.; Novais, G. L. Traditional and New methods for the Preparation of Diazocarbonyl Compounds. Anais da Academia Brasileira de Ciencias 2018, 90, 859–893. doi:10.1590/0001-3765201820170768
• Khan, M.; Misra, S.; Srivastava, R. C.; Chauhan, A. K.; Duthie, A.; Butcher, R. J. Piperidin-1-ylamidomethyltellurium derivatives: Synthesis and solid state structures. Inorganica Chimica Acta 2017, 462, 209–214. doi:10.1016/j.ica.2017.03.032
• Zhang, C.; Huang, J.; Qiu, L.; Xu, X. Thermally Induced [3 + 2] Cycloaddition of Alkynyl-Tethered Diazoamides: Synthetic and Mechanistic Insights. Organic letters 2016, 18, 6208–6211. doi:10.1021/acs.orglett.6b03288
• Mari, G.; Favi, G.; De Crescentini, L.; Santeusanio, S.; Attanasi, O. A.; Mantellini, F. Facile, Odourless, Quantitative Synthesis of 3‐Hydroxy‐3,4‐dihydro‐2H‐1,4‐thiazines. Asian Journal of Organic Chemistry 2016, 5, 705–709. doi:10.1002/ajoc.201600115
• Shimokawa, J.; Fukuyama, T. N,N′-Bis(p-toluenesulfonyl)hydrazine. Encyclopedia of Reagents for Organic Synthesis 2016, 1–2. doi:10.1002/047084289x.rn01898
• Wang, X.; Dong, K.; Yan, B.; Zhang, C.; Qiu, L.; Xu, X. NBS-mediated dinitrogen extrusion of diazoacetamides under catalyst-free conditions: practical access to 3-bromooxindole derivatives. RSC Advances 2016, 6, 70221–70225. doi:10.1039/c6ra16868j
• Giedyk, M.; Goliszewska, K.; Proinsias, K. ó.; Gryko, D. Cobalt(I)-catalysed CH-alkylation of terminal olefins, and beyond. Chemical communications (Cambridge, England) 2015, 52, 1389–1392. doi:10.1039/c5cc07363d
• Tarui, A. 多置換フルオロ-β-ラクタム類の立体選択的合成と含フッ素β-アミノ酸骨格への変換. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 2015, 135, 1245–1253. doi:10.1248/yakushi.15-00201
• Ford, A.; Miel, H.; Ring, A.; Slattery, C. N.; Maguire, A. R.; McKervey, M. A. Modern Organic Synthesis with α-Diazocarbonyl Compounds. Chemical reviews 2015, 115, 9981–10080. doi:10.1021/acs.chemrev.5b00121
• Dong, Z.; Xiao, X.-Q.; Li, Z.; Lu, Q.; Lai, G.; Kira, M. Elusive 2H-1,2-oxasiletes through reactions of an isolable dialkylsilylene with diazocarbonyl compounds. Organic & biomolecular chemistry 2015, 13, 9471–9476. doi:10.1039/c5ob01224d

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