Pu, X., Li, Q., Lu, Z., Yang, X. (2016). N-Chloro-N-methoxybenzenesulfonamide: A Chlorinating Reagent. Eur. J. Org. Chem., (36), 5937−5940. https://doi.org/10.1002/ejoc.201601226

Glover, S. A. (1998). Anomeric Amides – Structure, Properties and Reactivity. Tetrahedron, 54(26), 7229–7271. https://doi.org/10.1016/S0040-4020(98)00197-5

Brink, K., Mattes, R. (1985). Mesylhydroxylamine. VII. Chlorierte mesylhydroxylamine. Chem.-Ztg., 109 (1), 10−11.

Shtamburg, V.G., Shishkin, O.V., Zubatyuk, R.I., Kravchenko, S.V., Tsygankov, A.V., Mazepa, A.V., Klots, E.A., Kostyanovsky, R.G. (2006).N-Chloro-N-alkoxyureas: synthesis, structure and properties. Mendeleev Commun., 16(6), 323–325. https://doi.org/10.1070/MC2006v016n06ABEH002382

Shtamburg, V.G., Shishkin, O.V., Zubatyuk R.I., Kravchenko, S.V., Shtamburg, V.V., Distanov, V.B., Tsуgankov A.V., Kostyanovsky, R.G.(2007). Synthesis,structure and properties of N-alkoxy-N-(1-pyridinium)urea salts, N-alkoxy-N-acyloxyureas and N,N-dialkoxyureas.Mendeleev Commun.,17(3), 178–180. https://doi.org/10.1016/j.mencom.2007.05.016

Shishkin, O.V., Shtamburg, V.G., Zubatyuk R.I., Olefir, D.A., Tsygankov, A.V., Prosyanik, A.V., Mazepa, A.V., Kostyanovsky, R.G. (2009). Chiral Ureas with Two Electronegative Substituents at 1-N and Unusual Case of Coexisting a Pyramidal and Almost Planar 1-N in The Same Crystal. Chirality, 21(7). 642–647. https://doi.org/10.1002/chir.20668

Shtamburg, V.G., Tsygankov, A.V., Gerasimenko, M.V., Shishkin, O.V., Zubatyuk, R.I., Mazepa, A.V.; Kostyanovsky, R.G. (2011).New approach to N,N-dialkoxy-N'-arylureas and N,N-dialkoxycarbamates. Mendeleev Commun., 21(12), 50−32. https://doi.org/10.1016/j.mencom.2011.01.021

Shtamburg, V.G., Tsygankov, A.V., Shishkin,O.V., Zubatyuk, R.I., Uspensky, B.V., Shtamburg,V.V., Mazepa, A.V., Kostyanovsky, R.G. (2012).The properties and structure of N-chloro-N-methoxy-4-nitrobenzamide. Mendeleev Commun., 22(3), 164–166. https://doi.org/10.1016/j.mencom.2012.05.019

Glover, S. A., Rosser, A. A. (2018). Heteroatom Substitution at Amide Nitrogen – Resonance Reduction and HERON Reactions of Anomeric Amides. Molecules, 23(11), 2834. https://doi.org/10.3390/molecules23112834

Glover, S. A. (2009). N-Heteroatom-substituted hydroxamic esters, in The Chemistry of Hydroxylamines, Oximes and Hydroxamic Acids. Eds Rappoport, Z., Liebman, J. F., John Wiley and Sons, New York. PATAI’S Chemistry of Funcional Groups, 839–923. https://doi.org/10.1002/9780470682531.pat0470

Wang, Yu., Kawamata, Yu., Grant, L. N., Samp, L., Richardson, P. F., Zhang, S., Harper, K. C., Palkowitz, M.D., Vasilopoulos, A., Collins, M. R., Oderinde, M. S., Tyrol, C.C., Chen, D., LaChapelle, E. A., Bailey, J. B., Qiao, J. X., Baran, P. S. (2024). Discovery of N−X anomeric amides as electrophilic halogenation reagents. Nature Chemistry, 16, 1539−1545. https://doi.org/10.1038/s41557-024-01539-4

Garg, A., Vigier, J., Lebel, H., Besset, T.(2026). Anomeric Amides: Valuable reagents in Synthetic Organic Chemistry. Angew. Chem. Int. Ed. 65(12), e25799. https://doi.org/10.1002/anie.202525799

Kim, M., Obertone, C., Kelly, C., Reiher, S.A., Grosanu, S., Robertson, J.C., Levin M.D.(2025). Accesing Sulfonamides via Formal SO2 Insertion Into C–N Bonds. Nature Chemistry, 17, 1247–1255. https://doi.org/10.1038/s41557-025-01848-2

Kwon, J.-D., Joaquin, D., Davenport, M.T., Olsen, J., Carpio, M., Yousufuddin, M., Ess, D.H., Kurti, L. (2026) Polar-to-Radical Crossover in Catalyst-Free Olefin Halo-Hydroxylamination: Rapid Synthesis of Multifunctional Electrofilic Hydroxylamines. JACS Au, 6(1), 521−523. https://doi.org/10.1021/jacsau.5c01471

Stein, C.,Tyler, J.L., Wiener, J., Boser, F., Daniliuc, C.G., Glorius, F. Anomeric Amide-Enable Alkene-Arene and Alkene-Alkene Aminative Coupling. (2025). Angew. Chem. Int. Ed. 64(5), e202418141. https://doi.org/10.1002/anie.202418141

Kravchenko, S.V. (2013). N-Chloro-N-benzoyloxybenzamide. Bull. Dnipropetrovsk Univ.Ser. Chem., 21(19), 61−65.https://doi.org/10.15421/08132119

Shtamburg, V.G., Klots, EA., Shtamburg, V.V., Anishchenko, A.A., Shishkina, S. V., Kravchenko, S.V. Mazepa, A.V. (2025). Dialkyl N-Alkoxy-N-(4-toluenesulfonyl)phosphoramidates: Synthesis and Structure. Voprosy khimii i khimicheskoi tecknologii – Issues of Chemistry and Chemical Technology, (2), 33−44. http://dx.doi.org/10.32434/0321-4095-2025-159-2-33-44

Shtamburg, V.G., Klots, EA., Shtamburg, V.V., Anishchenko, A.A., Shishkina, S. V., Kravchenko, S.V., Mazepa, A.V. (2024). Structure of N-acetoxy-N-benzyloxyurea. Voprosy khimii i khimicheskoi tecknologii – Issues of Chemistry and Chemical Technology, (2), 88−44. http://dx.doi.org/10.32434/0321-4095-2024-155-4-88-94 10.32434/0321–4095–2024–155–4–88–94

Shtamburg, V.G., Anishchenko A. A., Klots, E.A., Shishkina, S.V., Kravchenko, S.V., Mazepa, A.V., Sokolova L.A., Krishchik O.V. (2024). N-Benzyloxy-N-methoxyurea. Synthesis and Structure. J. of Chemistry and Technologies, 32(1), 56−64. https://doi.org/10.15421/jchemtech.v32i1.292868

Wu, S., Chen, P., Duan, M., Jiang, P.-Y., Zhou, Xiang, Q. S.-H., Houk, K.N., Tan, B. (2025). Controlling pyramidal nitrogen chirality by asymmetric organocatalysis. Nature, 12, Nov. https://www.nature.com/articles/s41586-025-09607-6

Dolomanov, O.B., Bourhis, L.J., Gildea, R.J.,

Howard, J.A.K., Puschmann, H. OLEX2: a complete structure solution, refinement and analysis program. (2009). J. Appl. Crystallogr., 42, 339–341. https://doi.org/10.1107/S0021889808042726

Sheldrick, G. M. SHELXT – Integrated space-group and crystal-structure determination. (2015). Acta Cryst., Sect. A., A 71, P.1, 3−8. https://doi.org/10.1107/S2053273314026370

Sheldrick, G.M. Crystal Structure Refinement with SHELXL. (2015). Acta Crystallogr. Sect. C, 71, 3–8. http://dx.doi.org/10.1107/S2053229614024218

Kanishchev, O.S., Shermolovich, Yu.G. Synthetic Methods and Properties of N-Halogenoazoles. (2011). J. Org. Pharm. Chem., 9(3), 15−35.