Jump to main content
Jump to site search

Issue 5, 2010
Previous Article Next Article

A facile and efficient one-pot synthesis of polysubstituted benzenes in guanidinium ionic liquids

Author affiliations

Abstract

A facile and efficient synthesis of polysubstituted benzenes has been developed via sequential Michael addition, Knoevenagel condensation and nucleophilic cyclization reactions of readily available chalcones with active methylene compounds in guanidinium ionic liquids.

Graphical abstract: A facile and efficient one-pot synthesis of polysubstituted benzenes in guanidinium ionic liquids

Back to tab navigation

Supplementary files

Publication details

The article was received on 14 Oct 2009, accepted on 19 Feb 2010 and first published on 23 Mar 2010


Article type: Paper
DOI: 10.1039/B921390B
Green Chem., 2010,12, 893-898

  •   Request permissions

    A facile and efficient one-pot synthesis of polysubstituted benzenes in guanidinium ionic liquids

    X. Xin, Y. Wang, W. Xu, Y. Lin, H. Duan and D. Dong, Green Chem., 2010, 12, 893
    DOI: 10.1039/B921390B

Search articles by author

Spotlight

Advertisements