Synthesis, structure and reactivity of 4-phosphanylated 1,3-dialkyl-imidazole-2-thiones

Dalton Trans. 2012 May 7;41(17):5368-76. doi: 10.1039/c2dt12483a. Epub 2012 Mar 7.

Abstract

Selective formation of 4-phosphanylated 1,2-dialkyl imidazole-2-thiones 3a-f has been obtained via a lithiation followed by phosphanylation reaction. The reactivity of 3a-f was examined towards oxidation and complexation reactions. All products were unambiguously characterized by elemental analyses, spectroscopic and spectrometric methods including X-ray analysis (3a, 3b, 4b, 4d, 5b, 6a and 6d).

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Chemistry Techniques, Synthetic / methods*
  • Imidazoles / chemistry*
  • Oxidation-Reduction
  • Phosphines / chemistry*
  • Thiones / chemical synthesis*
  • Thiones / chemistry*

Substances

  • Imidazoles
  • Phosphines
  • Thiones
  • phosphine