期刊文献+

VO(acac)_2 catalyzed condensation of o-phenylenediamine with aromatic carboxylic acids/aldehydes under microwave radiation affording benzimidazoles 被引量:2

VO(acac)_2 catalyzed condensation of o-phenylenediamine with aromatic carboxylic acids/aldehydes under microwave radiation affording benzimidazoles
原文传递
导出
摘要 Vanadyl acetylacetonate,VO(acac)_2,has been found to be very effective catalyst for synthesis of a variety of benzimidazoles under solvent-free condition.The methodology involves the exposure of a mixture of o-phenylenediamine and a selected aromatic carboxylic acid/aldehyde to microwave radiation without the use of any solvent or supporting agents.The benzimidazoles were obtained in quick time with high yields. Vanadyl acetylacetonate,VO(acac)_2,has been found to be very effective catalyst for synthesis of a variety of benzimidazoles under solvent-free condition.The methodology involves the exposure of a mixture of o-phenylenediamine and a selected aromatic carboxylic acid/aldehyde to microwave radiation without the use of any solvent or supporting agents.The benzimidazoles were obtained in quick time with high yields.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第3期296-299,共4页 中国化学快报(英文版)
基金 the Department of Science and Technology(DST),New Delhi,Government of India for providing financial support(SR/FTP/CS-100/2007)
关键词 Vanadyl acetylacetonate O-PHENYLENEDIAMINE Microwave irradiation SOLVENT-FREE Vanadyl acetylacetonate o-Phenylenediamine Microwave irradiation Solvent-free
  • 相关文献

参考文献22

  • 1D.K. Maiti, S. Halder, P. Pandit, et al. J. Org. Chem. 74 (2009) 8086.
  • 2R.S. Keri, K.M. Hosamani, H.R. Seetharama Reddy, et al. Catal. Lett. 131 (2009) 552.
  • 3T. Fonseca, B. Gigante, T.L. Gilchrist, Tetrahedron 57 (2001) 1793.
  • 4C. Pabba, H.J. Wang, S.R. Mulligan, et al. Tetrahedron Lett. 46 (2005) 7553.
  • 5W.A. Denny, G.W. Rewcastle, B.C. Baguley, J. Med. Chem. 33 (1990) 814.
  • 6M.R. Maurya, N. Bharti, Transit. Met. Chem. 24 (1999) 389.
  • 7M. Alamgir, D.St.C. Black, N. Kumar, Top. Heterocycl. Chem. 9 (2007) 87.
  • 8K. Bahrami, M.M. Khodaei, E Naali, J. Org. Chem. 73 (2008) 6835.
  • 9R.R. Nagawade, D.B. Shinde, Chin. Chem. Lett. 17 (2006) 453.
  • 10K. Bougrin, A. Loupi, A. Petit, et al. Tetrahhedron 57 (2001) 163.

同被引文献11

引证文献2

二级引证文献11

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