期刊文献+

The efficient synthesis of 14-alkyl or aryl 14H-dibenzo[a,j] xanthenes catalyzed by bismuth(Ⅲ)chloride under solvent-free conditions 被引量:1

The efficient synthesis of 14-alkyl or aryl 14H-dibenzo[a,j]xanthenes catalyzed by bismuth(Ⅲ)chloride under solvent-free conditions
原文传递
导出
摘要 An efficient method for the synthesis of 14-alkyl or aryl 14H-dibenzo[a,j]xanthene derivatives by the reaction of β-naphthol,and aldehydes in the presence of a catalytic amount of bismuth(Ⅲ) chloride(BiCl_3) under solvent-free conditions at 110℃is described.Aliphatic and aromatic aldehydes were used in the reaction and in all cases the desired products were synthesized successfully.This reaction was studied under different temperatures;the maximum yield was obtained in a short reaction period at 110℃.The method offers the advantages of high yields,short reaction times,simplicity and easy workup compared to the conventional method of syntheses. An efficient method for the synthesis of 14-alkyl or aryl 14H-dibenzo[a,j]xanthene derivatives by the reaction of β-naphthol,and aldehydes in the presence of a catalytic amount of bismuth(Ⅲ) chloride(BiCl_3) under solvent-free conditions at 110℃is described.Aliphatic and aromatic aldehydes were used in the reaction and in all cases the desired products were synthesized successfully.This reaction was studied under different temperatures;the maximum yield was obtained in a short reaction period at 110℃.The method offers the advantages of high yields,short reaction times,simplicity and easy workup compared to the conventional method of syntheses.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第8期927-930,共4页 中国化学快报(英文版)
基金 financial support from the Research Council of Razi University
关键词 Bismuth(Ⅲ) chloride 14H-Dibenzo[a j]xanthenes Β-NAPHTHOL Bismuth(Ⅲ) chloride 14H-Dibenzo[a j]xanthenes β-Naphthol
  • 相关文献

参考文献24

  • 1E.E Llama, C. Campo, M. Capo, M. Anadon, Eur. J. Med. Chem. 24 (1989) 391.
  • 2Y. Kitahara, K. Tanaka, Chem. Commun. (2002) 932.
  • 3R.M. Ion, D. Frackowiak, A. Planner, K. Wiktorowicz, Acta Biochim. Pol. 45 (1998) 833.
  • 4O. Sirkecioglu, N. Tulinli, A. Akar, J. Chem. Res. Synop. (1995) 502.
  • 5D. Quintas, A. Garcia, D. Dominguez, Chem. Inform. 35 (2004) 154.
  • 6D.W. Knight, EB. Little, Synlett (1998) 1141.
  • 7A. Jha, J. Beal, Tetrahedron Lett. 45 (2004) 8999.
  • 8A. Bekaert, J. Andrieux, M. Plat, Tetrahedron Lett. 33 (1992) 2805.
  • 9J.A. Van Allan, D.D. Giannini, T.H. Whitesides, J. Org. Chem. 47 (1982) 820.
  • 10P. Papini, R. Cimmarusti, Gazz. Chim. Ital. 77 (1947) 142.

同被引文献5

引证文献1

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