Journal article

Publication year: 2007

Pages: 2825-2838

Journal: European Journal of Organic Chemistry

Volume number: 2007

Issue number: 17

ISSN: 1434-193X

DOI Link: https://doi.org/10.1002/ejoc.200700114

Publisher: Wiley

Abstract: 

1‐Alkyl‐3‐methylimidazole‐2‐thiones were prepared from amino esters in
one pot and converted to inherently halide‐free
1‐alkyl‐3‐methylimidazolium benzoates by oxidation with benzoyl peroxide
followed by a novel anion exchange. Also reported are the outcomes of
exchanges with other anions, acidifications of the imidazolium benzoates
to other salts, and extension of the method to the syntheses of
1,3‐diphenylimidazolium and 3‐methyl‐ and ‐butylthiazolium salts.

Harvard Citation style: Wolfe, D. and Schreiner, P. (2007) Oxidative Desulfurization of Azole‐2‐thiones with Benzoyl Peroxide: Syntheses of Ionic Liquids and Other Azolium Salts, European Journal of Organic Chemistry, 2007(17), pp. 2825-2838. https://doi.org/10.1002/ejoc.200700114

APA Citation style: Wolfe, D., & Schreiner, P. (2007). Oxidative Desulfurization of Azole‐2‐thiones with Benzoyl Peroxide: Syntheses of Ionic Liquids and Other Azolium Salts. European Journal of Organic Chemistry. 2007(17), 2825-2838. https://doi.org/10.1002/ejoc.200700114