N-Arylcyanothioformamides: Preparation Methods and Application in the Synthesis of Bioactive Molecules

Ziad Moussa*, Zaher M.A. Judeh, Marwa A.M.Sh El-Sharief, Ahmed M.Sh El-Sharief

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

7 Citations (Scopus)

Abstract

This comprehensive review discusses the various preparation methods of N-arylcyanothioformamides and highlights the diverse chemistry and application of such reagents in organic synthesis since they were first reported. Specifically, the review describes applications of the preceding reagents in the preparation of the highly bioactive heterocyclic imidazolidineiminothiones, bis-imidazolidineiminothiones and derivatives thereof. The review also demonstrates how N-arylcyanothioformamides provide access to the highly coveted luciferin analogues for bioluminescence imaging applications. As well, the review showcases the metal complexation chemistry of N-arylcyanothioformamides and the regiochemical outcome of its reactions with isocyanates versus isothiocyanates. Many examples are provided from the literature to show the scope and selectivity (regio, stereo, and chemo) in these transformations.

Original languageEnglish
Pages (from-to)764-798
Number of pages35
JournalChemistrySelect
Volume5
Issue number2
DOIs
Publication statusPublished - Jan 16 2020
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

ASJC Scopus Subject Areas

  • General Chemistry

Keywords

  • Appel's salt
  • Heterocyclic synthesis
  • Imidazolidineiminothiones.
  • Isocyanates
  • Isothiocyanates
  • N-arylcyanothioformamides

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