[1] T. Janecki, Natural Lactones and Lactams: Synthesis, occurrence and biological activity, John Wiley & Sons (2013).
[2] (a) M. Carlier, V. Stove, S.C. Wallis, J.J. De Waele, A.G. Verstraete, J. Lipman, J.A. Roberts, Assays for therapeutic drug monitoring of β-lactam antibiotics: a structured review, International journal of antimicrobial agents 46 (2015) 367-375; (b) J. Caruano, G. Muccioli, R. Robiette, Biologically active γ-lactams: synthesis and natural sources, Org. Biomol. Chem., 14 (2016) 10134-10156.
[3] (a) K. Hashimoto, Ring-opening polymerization of lactams. Living anionic polymerization and its applications, Prog. Polym. Sci., 25 (2000) 1411-1462; (b) O. Nuyken, S.D. Pask, Ring-opening polymerization—An introductory review, Polymers, 5 (2013) 361-403.
[4] (a) H.M.A. Hassan, Recent applications of ring-closing metathesis in the synthesis of lactams and macrolactams, Chem. Commun., 46 (2010) 9100-9106; (b) A. Albrecht, Ł. Albrecht, T. Janecki, Recent advances in the synthesis of α‐alkylidene‐substituted δ‐lactones, γ‐lactams and δ‐lactams, Eur. J. Org. Chem., (2011) 2747-2766; (c) L.-W. Ye, C. Shu, F. Gagosz, Recent progress towards transition metal-catalyzed synthesis of γ-lactams, Org. Biomol. Chem., 12 (2014) 1833-1845.
[5] (a) J. Wang, P. Su, S. Abdolmohammadi, E. Vessally, A walk around the application of nanocatalysts for cross-dehydrogenative coupling of C–H bonds, RSC Adv., 9 (2019) 41684-41702; (b) S. Ebrahimiasl, F. Behmagham, S. Abdolmohammadi, R.N. Kojabad, E. Vessally, Recent advances in the application of nanometal catalysts for Glaser coupling, Curr. Org. Chem. 23 (2019) 2489-2503.
[6] (a) A. Hosseinian, S. Ahmadi, F.A.H. Nasab, R. Mohammadi, E. Vessally, Cross-dehydrogenative C–H/S–H coupling reactions, Top. Curr. Chem., 376 (2018) 39; (b) W. Peng, E. Vessally, S. Arshadi, A. Monfared, A. Hosseinian, L. Edjlali, Cross-dehydrogenative coupling reactions between C (sp)–H and X–H (X= N, P, S, Si, Sn) bonds: An environmentally benign access to heteroatom-substituted alkynes, Top. Curr. Chem., 377(4) (2019) 20; (c) S. Arshadi, A. Banaei, A. Monfared, S. Ebrahimiasl, A. Hosseinian, Cross-dehydrogenative coupling reactions between arenes (C–H) and carboxylic acids (O–H): a straightforward and environmentally benign access to O-aryl esters, RSC Adv., 9 (2019) 17101-17118; (d) J. Chen, F.R. Sheykhahmad, Intramolecular cross‐dehydrogenative coupling of benzaldehyde derivatives: A novel and efficient route to benzocyclic ketones, J. Chin. Chem. Soc., (2019) DOI: 10.1002/jccs.201900214; (e) Y. Yang, D. Zhang, E. Vessally, Direct amination of aromatic C-H bonds with free amines, Top. Curr. Chem., 378 (2020) 37-37.
[7] (a) A. Hosseinian, S. Farshbaf, L.Z. Fekri, M. Nikpassand, E. Vessally, Cross-dehydrogenative coupling reactions between P(O)–H and X–H (X= S, N, O, P) bonds, Top. Curr. Chem., 376(3) (2018) 23; (b) F.A.H. Nasab, L.Z. Fekri, A. Monfared, A. Hosseinian, E. Vessally, Recent advances in sulfur–nitrogen bond formation via cross-dehydrogenative coupling reactions, RSC Adv., 8 (2018) 18456-18469.
[8] E. Vessally, M. Babazadeh, A. Hosseinian, L. Edjlali, L. Sreerama, Recent advances in synthesis of functionalized β-lactams through cyclization of N-propargyl amine/amide derivatives, Curr. Org. Chem. 22 (2018) 199-205.
[9] S. Soleimani-Amiri, E. Vessally, M. Babazadeh, A. Hosseinian, L. Edjlali, Intramolecular cyclization of N-allyl propiolamides: a facile synthetic route to highly substituted γ-lactams (a review), RSC Adv., 7 (2017) 28407-28418.
[10] (a) A. Hosseinian, F.A.H. Nasab, S. Ahmadi, Z. Rahmani, E. Vessally, Decarboxylative cross-coupling reactions for P(O)–C bond formation, RSC Adv., 8 (2018) 26383-26398; (b) S. Arshadi, S. Ebrahimiasl, A. Hosseinian, A. Monfared, E. Vessally, Recent developments in decarboxylative cross-coupling reactions between carboxylic acids and N–H compounds, RSC Adv., 9 (2019) 8964-8976; (c) Y. Liu, A.G. Ebadi, L. Youseftabar-Miri, A. Hassanpour, E. Vessally, Methods for direct C (sp 2)–H bonds azidation, RSC Adv., 9 (2019) 25199-25215; (d) C. Yang, A. Hassanpour, K. Ghorbanpour, S. Abdolmohammadi, E. Vessally, Recent advances in direct trifluoromethylation of olefinic C–H bonds, RSC Adv., 9 (2019) 27625-27639.
[11] T. Naota, S.-I. Murahashi, Ruthenium-catalyzed transformations of amino alcohols to lactams, Synlett, (1991) 693-694.
[12] L.U. Nordstrøm, H. Vogt, R. Madsen, Amide synthesis from alcohols and amines by the extrusion of dihydrogen, J. Am. Chem. Soc., 130 (2008) 17672-17673.
[13] S.C. Ghosh, S.H. Hong, Simple RuCl3‐catalyzed amide synthesis from alcohols and amines, Eur. J. Org. Chem., (2010) 4266-4270.
[14] B. Saha, G. Sengupta, A. Sarbajna, I. Dutta, J.K. Bera, Amide synthesis from alcohols and amines catalyzed by a RuII–N-heterocyclic carbene (NHC)–carbonyl complex, J. Organomet. Chem., 771 (2014) 124-130.
[15] S.C. Ghosh, S. Muthaiah, Y. Zhang, X. Xu, S.H. Hong, Direct amide synthesis from alcohols and amines by phosphine‐free ruthenium catalyst systems, Adv. Synth. Catal., 351(16) (2009) 2643-2649.
[16] S. Muthaiah, S.C. Ghosh, J.-E. Jee, C. Chen, J. Zhang, S.H. Hong, Direct amide synthesis from either alcohols or aldehydes with amines: activity of Ru (II) hydride and Ru (0) complexes, J. Org. Chem., 75 (2010) 3002-3006.
[17] C. Chen, Y. Zhang, S.H. Hong, N-heterocyclic carbene based ruthenium-catalyzed direct amide synthesis from alcohols and secondary amines: Involvement of esters, J. Org. Chem., 76 (2011) 10005-10010.
[18] J.H. Dam, G. Osztrovszky, L.U. Nordstrøm, R. Madsen, Amide synthesis from alcohols and amines catalyzed by ruthenium N‐heterocyclic carbene complexes, Chem. Eur. J., 16 (2010) 6820-6827.
[19] Y. Zhang, C. Chen, S.C. Ghosh, Y. Li, S.H. Hong, Well-defined N-heterocyclic carbene based ruthenium catalysts for direct amide synthesis from alcohols and amines, Organometallics, 29 (2010) 1374-1378.
[20] B.P. Babu, Y. Endo, J.E. Bäckvall, Biomimetic aerobic oxidation of amino alcohols to lactams, Chem. Eur. J., 18 (2012) 11524-11527.
[21] D. Pingen, D. Vogt, Amino-alcohol cyclization: selective synthesis of lactams and cyclic amines from amino-alcohols, Catal. Sci. Technol., 4 (2014) 47-52.
[22] K.-i. Fujita, Y. Takahashi, M. Owaki, K. Yamamoto, R. Yamaguchi, Synthesis of five-, six-, and seven-membered ring lactams by Cp*Rh complex-catalyzed oxidative N-heterocyclization of amino alcohols, Org. Lett., 6 (2004) 2785-2788.
[23] Y. Wang, D. Zhu, L. Tang, S. Wang, Z. Wang, Highly efficient amide synthesis from alcohols and amines by virtue of a water‐soluble gold/DNA catalyst, Angew Chem. Int. Ed. Engl., 50 (2011) 8917-8921.
[24] J-F. Soulé, H. Miyamura, S. Kobayashi, Powerful amide synthesis from alcohols and amines under aerobic conditions catalyzed by gold or gold/iron, -nickel or –cobalt nanoparticles, J. Am. Chem. Soc. 133 (2011) 18550–18553.
[25] J. Zhu, Y. Zhang, F. Shi, Y. Deng, Dehydrogenative amide synthesis from alcohol and amine catalyzed by hydrotalcite-supported gold nanoparticles, Tetrahedron Lett., 53 (2012) 3178–3180.
[26] S. Kegnæs, J. Mielby, U. V. Mentzel, T. Jensen, P. Fristrup, A. Riisager, One-pot synthesis of amides by aerobic oxidative coupling of alcohols or aldehydes with amines using supported gold and base as catalysts, Chem. Commun., 48 (2012) 2427–2429.
[27] J-F. Soulé, H. Miyamura, S. Kobayashi, Selective lactam formation from amino alcohols using polymerIncarcerated gold and gold/cobalt nanoparticles as catalysts under aerobic oxidative conditions, Asian J. Org. Chem., 1 (2012) 319–321.
[28] M. Peña-López, H. Neumann, M. Beller, Iron(II) pincer-catalyzed synthesis of lactones and lactams through a versatile dehydrogenative domino sequence, ChemCatChem., 7 (2015) 865-871.
[29] S. Herter, S.M. McKenna, A.R. Frazer, S. Leimkìhler, A.J. Carnell, N.J. Turner, Galactose oxidase variants for the oxidation of amino alcohols in enzyme cascade synthesis, ChemCatChe., 7 (2015) 2313 –2317.
[30] L. Huang, G.V. Sayoga, F. Hollmann, S. Kara, Horse liver alcohol dehydrogenase-catalyzed oxidative lactamization of amino alcohols, ACS Catal., 8 (2018) 8680-8684.