Synthetic methods for the construction of cycl[3.2.2]azine molecules

References

• Boekelheide, V.; Windgassen, R. J. J. Am. Chem. Soc. 1958, 80, 2020–2020. DOI: 10.1039/b612166g.
   Google Scholar
• Windgassen, R. J.; Saunders, W. H.; Boekelheide, V. J. Am. Chem. Soc. 1959, 81, 1459–1465. DOI: 10.1021/ja01515a045.
   Web of Science ®Google Scholar
• Wu, Z. l.; Wang, Q.; Wang, J. X.; Dong, H. Y.; Xu, X. K.; Shen, Y. H.; Li, H. l.; Zhang, W. D. Org. Lett. 2018, 20, 7567–7570. DOI: 10.1021/acs.orglett.8b03306.
   PubMed Web of Science ®Google Scholar
• Ondrus, A. E.; Movassaghi, M. Chem. Commun. 2009, 45, 4151–4165. DOI: 10.1039/b903995n.
   Google Scholar
• Jørgensen, A. S.; Jacobsen, P.; Christiansen, L. B.; Bury, P. S.; Kanstrup, A.; Thorpe, S. M.; Bain, S.; Naerum, L.; Wassermann, K. Bioorg. Med. Chem. Lett. 2000, 10, 399–402. DOI: 10.1016/s0960-894x(00)00015-9.
   PubMed Web of Science ®Google Scholar
• Jørgensen, A. S.; Jacobsen, P.; Christiansen, L. B.; Bury, P. S.; Kanstrup, A.; Thorpe, S. M.; Naerum, L.; Wassermann, K. Bioorg. Med. Chem. Lett. 2000, 10, 2383–2386. DOI: 10.1016/s0960-894x(00)00474-1.
   PubMed Web of Science ®Google Scholar
• Mitsumori, T.; Bendikov, M.; Dautel, O.; Wudl, F.; Shioya, T.; Sato, H.; Sato, Y. J. Am. Chem. Soc. 2004, 126, 16793–16803. DOI: 10.1021/ja049214x.
   PubMed Web of Science ®Google Scholar
• Yang, D. T.; Radtke, J.; Mellerup, S. K.; Yuan, K.; Wang, X.; Wagner, M.; Wang, S. Org. Lett. 2015, 17, 2486–2489. DOI: 10.1021/acs.orglett.5b00994.
   PubMed Web of Science ®Google Scholar
• Snyder, S. A.; ElSohly, A. M.; Kontes, F. Angew. Chem. 2010, 122, 9887–9892. DOI: 10.1002/ange.201005825.
   Google Scholar
• Jessen, N. I.; Bertuzzi, G.; Bura, M.; Skipper, M. L.; Jørgensen, K. A. J. Am. Chem. Soc. 2021, 143, 6140–6151. DOI: 10.1021/jacs.1c00499.
   PubMed Web of Science ®Google Scholar
• Jessen, N. I.; Bura, M.; Bertuzzi, G.; Jørgensen, K. A. Angew. Chem. Int. Ed. Engl. 2021, 60, 18527–18531. DOI: 10.1002/anie.202106287.
   PubMed Web of Science ®Google Scholar
• Bertuzzi, G.; Corti, V.; Izzo, J. A.; Ricko, S.; Jessen, N. I.; Jørgensen, K. A. J. Am. Chem. Soc. 2022, 144, 1056–1065. DOI: 10.1021/jacs.1c12619.
   PubMed Web of Science ®Google Scholar
• Acheson, R. M.; Robinso, D. A. Chem. Commun. 1967, 3, 175–176. DOI: 10.1039/c19670000175.
   Google Scholar
• Flitsch, W.; Heinrich, J. Tetrahedron. Lett. 1980, 21, 3675–3676.
   Google Scholar
• Uchida, T.; Matsumoto, K. Chem. Lett. 1980, 9, 149–150. DOI: 10.1246/cl.1980.149.
   Google Scholar
• Abe, N.; Nishiwaki, T.; Yamamoto, H. Chem. Lett. 1982, 11, 805–806. DOI: 10.1246/cl.1982.805.
   Google Scholar
• Smith, J. O.; Mandal, B. K. J. Heterocyclic. Chem. 1997, 34, 1441–1446. DOI: 10.1002/jhet.5570340511.
   Web of Science ®Google Scholar
• Matsuda, Y.; Kohra, S.; Katou, K.; Itou, T.; Uemura, T. Heterocycles 1997, 45, 2223–2228. DOI: 10.3987/COM-97-7960.
   Web of Science ®Google Scholar
• Kuznetsov, A. G.; Bush, A. A.; Babaev, E. V. Tetrahedron. Lett. 2008, 64, 749–756. DOI: 10.1016/j.tet.2007.11.017.
   Google Scholar
• Shen, Y. M.; Grampp, G.; Leesakul, N.; Hu, H. W.; Xu, J. H. Eur. J. Org. Chem. 2007, 2007, 3718–3726. DOI: 10.1002/ejoc.200700250.
   Web of Science ®Google Scholar
• Gogoi, S.; Dutta, M.; Gogoi, J.; Boruah, R. C. Tetrahedron. Lett. 2011, 52, 813–816. DOI: 10.1016/j.tetlet.2010.12.036.
   Web of Science ®Google Scholar
• Zhurkina, F. E.; Pushkarev, V. E.; Tomilova, L. G. Curr. Org. Synth. 2015, 12, 378–384. DOI: 10.2174/1570179412666150318232315.
   Web of Science ®Google Scholar
• Hu, H. Y.; Li, G. D.; Hu, W. M.; Liu, Y.; Wang, X.; Kan, Y. H.; Ji, M. Org. Lett. 2015, 17, 1114–1117. DOI: 10.1021/ol503681n.
   PubMed Web of Science ®Google Scholar
• Liang, Y. F.; Teng, L. L.; Wang, Y. J.; He, Q. X.; Cao, H. Green Chem. 2019, 21, 4025–4029. DOI: 10.1039/c9gc01766f.
   Web of Science ®Google Scholar
• Zhang, Y.; Yu, Y.; Liang, B. B.; Pei, Y. Y.; Liu, X.; Yao, H. G.; Cao, H. J. Org. Chem. 2020, 85, 10719–10727. DOI: 10.1021/acs.joc.0c01253.
   PubMed Web of Science ®Google Scholar
• Huang, M. Z.; Deng, L. C.; Lao, T. F.; Zhang, Z. W.; Su, Z. Q.; Yu, Y.; Cao, H. J. Org. Chem. 2022, 87, 3265–3275. DOI: 10.1021/acs.joc.1c02940.
   PubMed Web of Science ®Google Scholar
• Belei, D.; Abuhaie, C.; Bicu, E.; Jones, P. G.; Hopf, H.; Birsa, L. M. Synlett 2012, 23, 545–548. DOI: 10.1055/s-0031-1290337.
   Google Scholar
• Cui, P. P.; Xu, L.; Shi, Z. J.; Gan, L. B. J. Org. Chem. 2011, 76, 4210–4212. DOI: 10.1021/jo200601y.
   PubMed Web of Science ®Google Scholar
• Liu, R. Z.; Wang, X. Y.; Sun, J.; Yan, C. G. Tetrahedron Lett. 2015, 56, 6711–6714. DOI: 10.1016/j.tetlet.2015.10.049.
   Web of Science ®Google Scholar
• Muranaka, H.; Kakehi, A.; Suga, H.; Itoh, K. Heterocycles 2010, 82, 1251–1266. DOI: 10.3987/COM-23-14826.
   Web of Science ®Google Scholar
• Kuzuhara, D.; Miyake, S.; Moriyama, H.; Tamura, Y.; Aratani, N.; Yamada, H. Tetrahedron Lett. 2015, 56, 5564–5567. DOI: 10.1016/j.tetlet.2015.08.044.
   Web of Science ®Google Scholar
• Chintawar, C.; Mane, M.; Tathe, A.; Biswas, S.; Patil, N. Org. Lett. 2019, 21, 7109–7113. DOI: 10.1021/acs.orglett.9b02677.
   PubMed Web of Science ®Google Scholar
• Liu, C.; Wu, S. N.; Sun, W.; Meng, H. F.; Xing, S. Y.; Zhu, B. L. Asian J. Org. Chem. 2020, 9, 68–72. DOI: 10.1002/ajoc.201900660.
   Web of Science ®Google Scholar
• Cembellín, S.; Maisuls, I.; Daniliuc, C.; Osthues, H.; Doltsinis, N.; Strassert, C.; Glorius, F. Org. Biomol. Chem. 2022, 20, 796–800. DOI: 10.1039/d1ob02246f.
   PubMed Web of Science ®Google Scholar