[1]
|
陶绍木, 张建华, 彭昌亚, 等. 杂环化合物的应用和发展[J]. 中国食品添加剂, 2003(3): 31-34.
|
[2]
|
Kumari, J. (2018) Application of Heterocyclic Compounds in Everyday Life. Journal of Modern Chemistry & Chemical Technology, 9, 1-7.
|
[3]
|
Saleh, S.S., Al-Salihi, S.S. and Mohammed, I.A. (2019) Biological Activity Study for Some Heterocyclic Compounds and Their Impact on the Gram Positive and Negative Bacteria. Energy Procedia, 157, 296-306.
https://doi.org/10.1016/j.egypro.2018.11.194
|
[4]
|
Jeffrey, C.S., Barnes, K.L., Eickhoff, J.A. and Carson, C.R. (2011) Generation and Reactivity of Aza-Oxyallyl Cationic Intermediates: Aza-[4 + 3] Cycloaddition Reactions for Heterocycle Synthesis. Journal of the American Chemical Society, 133, 7688-7691. https://doi.org/10.1021/ja201901d
|
[5]
|
Xuan, J., Cao, X. and Cheng, X. (2018) Advances in Heterocycle Synthesis via [3 + m]-cycloaddition Reactions Involving an Azaoxyallyl Cation as the Key Intermediate. Chemical Communications, 54, 5154-5163.
https://doi.org/10.1039/C8CC00787J
|
[6]
|
Jin, Q.-M., Gao, M., Zhang, D.-J., Jiang, C.-H., Yao, N. and Zhang, J. (2018) Base-Mediated [2 + 4] Cycloadditions of in Situ Formed Azaoxyallyl Cations with N-(2-chloromethyl) Aryl Amides. Organic & Biomolecular Chemistry, 16, 7336-7339. https://doi.org/10.1039/C8OB02176G
|
[7]
|
Ji, D.-Q. and Sun, J.-T. (2018) [3 + 2]-Cycloaddition of Azaoxyallyl Cations with Hexahydro-1, 3, 5-triazines: Access to 4-Imidazolidinones. Organic Letters, 20, 2745-2748. https://doi.org/10.1021/acs.orglett.8b00951
|
[8]
|
Eyilcim, O., Issever, S., Ocal, N., Gronert, S. and Erden, I. (2018) Imidazolidin-4-Ones via (3 + 2) Cycloadditions of Aza-Oxyallyl Cations onto (E)-N-arylideneanilines. Tetrahedron Letters, 59, 3674-3677.
https://doi.org/10.1016/j.tetlet.2018.08.056
|
[9]
|
Singh, R., Nagesh, K., Yugandhar, D. and Prasanthi, A.V.G. (2018) Metal- and Oxidant-Free Modular Approach to Access N-Alkoxy Oxindoles via Aryne Annulation. Organic Letters, 20, 4848-4853.
https://doi.org/10.1021/acs.orglett.8b01972
|
[10]
|
Li, J., Liu, S.-C., Niu, S.-B., Zhuang, W.-Y. and Che, Y.-S. (2009) Pyrrolidinones from the Ascomycete Fungus Albonectria rigidiuscula. Journal of Natural Products, 72, 2184-2187. https://doi.org/10.1021/np900619z
|
[11]
|
Ding, H., Wang, J.-N., Zhang, D.-S. and Ma, Z.-J. (2017) Derivatives of Holomycin and Cyclopropaneacetic Acid from Streptomyces sp. DT-A37. Chemistry & Biodiversity, 14, e1700140. https://doi.org/10.1002/cbdv.201700140
|
[12]
|
Zhang, Y.-X., Ma, H.-J., Liu, X.-X., Cui, X.-F., Wang, S.-H., Zhan, Z.-Z., Pu, J.-H. and Huang, G.-S. (2018) The Synthesis of Multi-Substituted Pyrrolidinones via a Direct [3 + 2] Cycloaddition of Azaoxyallyl Cations with Aromatic Ethylenes. Organic & Biomolecular Chemistry, 16, 4439-4442. https://doi.org/10.1039/C8OB00899J
|
[13]
|
Sun, S.-F., Chen, R.-X., Wang, G.-Q. and Wang, J. (2018) Sodium Carbonate Promoted [3 + 2] Annulation of Alpha-Halohydroxamates and Isocyanates. Organic & Biomolecular Chemistry, 16, 8011-8014.
https://doi.org/10.1039/C8OB02321B
|
[14]
|
Xu, X.-Y., Zhang, K.-F., Li, P.-P., Yao, H.-Q. and Lin, A.-J. (2018) [3 + 3] Cycloaddition of Azides with in Situ Formed Azaoxyallyl Cations to Synthesize 1, 2, 3, 4-Tetrazines. Organic Letters, 20, 1781-1784.
https://doi.org/10.1021/acs.orglett.8b00280
|
[15]
|
Wang, G.-Q., Chen, R.-X., Zhao, S., Yang, L.-F., Guo, H.-B., Sun, S.-F., Wang, J., Domena, J. and Xing, Y.-L. (2018) Efficient Synthesis of 1, 2, 4-Oxadiazine-5-Ones via [3 + 3] Cycloaddition of in Situ Generated Aza-Oxyallylic Cations with Nitrile Oxides. Tetrahedron Letters, 59, 2018-2020. https://doi.org/10.1016/j.tetlet.2018.04.025
|
[16]
|
Bell, I.M., Gallicchio, S.N., Wood, M.R., Quigley, A.G., Stump, C.A., Zartman, C.B., Fay, J.F., Li, C.C., Lynch, J.J., Moore, E.L., Mosser, S.D., Prueksaritanont, T., Regan, C.P., Roller, S., Salvatore, C.A., Kane, S.A., Vacca, J.P. and Selnick, H.G. (2018) Discovery of MK-3207: A Highly Potent, Orally Bioavailable CGRP Receptor Antagonist. ACS Medicinal Chemistry Letters, 1, 24-29. https://doi.org/10.1021/ml900016y
|
[17]
|
Kakarla, R., Liu, J., Naduthambi, D., Chang, W., Mosley, R.T., Bao, D., Steuer, H.M., Keilman, M., Bansal, S., Lam, A.M., Seibel, W., Neilson, S., Furman, P.A. and Sofia, M.J. (2014) Dis-covery of a Novel Class of Potent HCV NS4B Inhibitors: SAR Studies on Piperazinone Derivatives. Journal of Me-dicinal Chemistry, 57, 2136-2160.
https://doi.org/10.1021/jm4012643
|
[18]
|
Baldé, B., Force, G., Marin, L., Schulz, E., Gandon, V. and Lebœuf, D. (2018) Synthesis of Cyclopeta[b]piperazinones via an Azaoxyallyl Cation. Organic Letters, 20, 7405-7409. https://doi.org/10.1021/acs.orglett.8b03103
|
[19]
|
王刚, 何照林, 陈一, 等. 一种2H-1,4-噻嗪-3(4H)-酮衍生物的合成方法[P]. 中国专利, 201810616552.3. 2018-10-02.
|
[20]
|
Cheng, X., Cao, X., Zhou, S.-J., Cai, B.-G., He, X.-K. and Xuan, J. (2018) Transition-Metal Free Construction of Isoquinoline-Fused Triazines Containing Alkenyl C-X Bonds. Advanced Synthesis & Catalysis, 361, 1230-1235.
https://doi.org/10.1002/adsc.201801181
|