期刊文献+

One-pot synthesis of various xanthene derivatives using ionic liquid1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient and reusable catalyst under solvent-free conditions 被引量:4

One-pot synthesis of various xanthene derivatives using ionic liquid1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient and reusable catalyst under solvent-free conditions
原文传递
导出
摘要 In this study, 1,3-disulfonic acid imidazolium hydrogen sulfate (DSIMHS) is used as an efficient and reusable ionic liquid for the green, mild, and efficient synthesis of xanthenes under solvent-free conditions. Simple and easy work-up, low cost, green process, short reaction times and excellent yields of the products are the advantages of this procedure. Further, the catalyst can be recycled and reused at least for four times without a noticeably decrease in its catalytic activity. In this study, 1,3-disulfonic acid imidazolium hydrogen sulfate (DSIMHS) is used as an efficient and reusable ionic liquid for the green, mild, and efficient synthesis of xanthenes under solvent-free conditions. Simple and easy work-up, low cost, green process, short reaction times and excellent yields of the products are the advantages of this procedure. Further, the catalyst can be recycled and reused at least for four times without a noticeably decrease in its catalytic activity.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第2期341-347,共7页 中国化学快报(英文版)
基金 the University of Guilan Research Council for the partial support
关键词 Xanthene derivatives One-pot reaction 1 3-Disulfonic acid imidazolium hydrogensulfate Ionic liquid Solvent-free conditions Xanthene derivatives One-pot reaction 1,3-Disulfonic acid imidazolium hydrogensulfate Ionic liquid Solvent-free conditions
  • 相关文献

参考文献4

二级参考文献22

  • 1A.R. Khosropour, M.M. Khodaei, H. Moghannian, Synlett (2005) 955.
  • 2D.W. Knight, EB. Little, J. Chem. Soc., Perkin Trans. 1 (2001) 1771.
  • 3A. Jha, J. Beal, Tetrahedron Lett. 45 (2004) 8999.
  • 4C.W. Kuo, J.M. Fang, Synth. Commun. 31 (2001) 877.
  • 5R. Kumar, G.C. Nandi, R.K. Verma, et al. Tetrahedron Lett. 51 (20J0) 442.
  • 6M.H. Alizadeh, H. Razavi, EE Bamoharram, et al. J. Mol. Catal. 206 (2003) 89.
  • 7S. Allameh, M.M. Heravi, M.M. Hashemi, et al. Chin. Chem. Lett. 22 (2011) 131.
  • 8S. Allameh, M.M. Hashemi, M.M. Heravi, et al. Asian J. Chem. 23 (4) (2011) 1588.
  • 9I.V. Kozhevinikov, K.I. Matveev, Appl. Catal. 5 (1983) 135.
  • 10I.V. Kozhevinikov, Catal. Rev. Sci. Eng. 37 (2) (1995) 311.

共引文献11

同被引文献22

引证文献4

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部