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微波辐射下一步合成9-芳基-1,2,3,4,5,6,7,8,9,10-十氢-1,8-吖啶二酮 被引量:4

One-pot Synthesis of 9-Aryl-1,2,3,4,5,6,7,8,9,10-decahydro- 1,8-acridinedione under Microwave Irradiation
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摘要 以芳醛、1,3-环己二酮、醋酸铵为原料在无溶剂条件下经微波辐射合成了一系列9-芳基-1,2,3,4,5,6,7,8,9,10-十氢-1,8-吖啶二酮.该反应的反应时间短、产率高、环境友好、后处理方便.产物的结构经红外光谱、核磁共振谱表征,3d的结构经单晶X射线衍射进一步确证. A series of 9-aryl-1,2,3,4,5,6,7,8,9,10-decahydro-1,8-acridinedione derivatives were synthesized via the reaction of aromatic aldehydes with 1,3-cyclohexanedione and ammonium acetate in solvent-free conditions under microwave irradiation by one-pot reaction. The reaction easily could be worked up with short reaction time, high yields and environmental friendliness. The structures of the products were confinned by IR and ^1H NMR spectra. The structure of 3d was further determined by X-ray analysis.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2005年第10期1294-1297,共4页 Chinese Journal of Organic Chemistry
基金 国家自然科学基金(No.20372057) 江苏省自然科学基金(No.BK2001142) 江苏省苏州大学化学化工学院有机合成重点实验室开放基金(No.S8109111) 江苏省药用植物生物技术重点实验室开放基金(No.01AXL14)资助项目.
关键词 芳醛 1 3-环己二酮 吖啶二酮 微波辐射 微波辐射合成 环己二酮 一步合成 芳基 吖啶 单晶X射线衍射 aromatic aldehyde 1,3-cyclohexanedione microwave irradiation acridinedione
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  • 1Janis, R. A.; Silver, P. J.; Triggle, D. J. Adv. Drug Res.1987, 16, 309.
  • 2Bossert, F.; Vater, W. Med. Res. Rev. 1989, 9, 291.
  • 3Eisner, U.; Kuthan, J. Chem. Rev. 1972, 72, 1.
  • 4Stout, D. M.; Meyers, A. I. Chem. Rev. 1982, 82, 223.
  • 5Bossert, F.; Meyers, H.; Wehinger, E. Angew. Chem.,Int. Ed. Engl. 1981, 20, 762.
  • 6Kuthan, J.; Kurfurst, A. Ind. Eng. Chem. Prod. Res. Dev.1982, 211, 191.
  • 7Chorvat, R. J.; Rorig, K. J. J. Org. Chem. 1988, 53,5779.
  • 8Kappe, C. O.; Fabian, W. M. F. Tetrahedron 1997, 53,2803.
  • 9Kappe, C. O. Tetrahedron 1993, 49, 6937.
  • 10Goldman, S.; Geiger, W. Angew. Chem., Int. Ed. Engl.1984, 23, 301.

二级参考文献20

  • 1Sainani J B,Indian J Chem.B,1994年,33卷,526页
  • 2Zhang X Y,离子交换与吸附,1999年,15卷,374页
  • 3Janis, R. A.; Silver, P. J.; Triggle, D. J. Adv. Drug Res. 1987, 16, 309-591.
  • 4Eisner, U.; Kuthan, J. Chem. Rev. 1972, 72, 1.
  • 5Chorvat, R. J.; Rorig, K. J. J. Org. Chem. 1988, 53, 5779-5781.
  • 6Goldman, S.; Geiger, W. Angew. Chem. Int. Ed. Engl. 1984, 23, 301-302.
  • 7Schramm, N.; Thomas, G.; Towart, R.; Franckowaik, G. Nature 1983, 303, 535-537.
  • 8Martin, N.; Quinteiro, M.; Segura, J. L.; Seoane, C.; Soto, J. L.; Morales, M.; Suarez, M. Liebigs Ann. Chem. 1991, 827-830.
  • 9Mora, A.; Suarez, M.; Ochoa, E.; Morales, A.; Bosque, J. R. D. J. Heterocyclic Chem. 1995, 32, 235-238.
  • 10Suarez, M.; Loupy, A.; Salfran, E.; Moran, L.; Rolando, E. Heterocycles 1999, 51, 21-27.

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