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 language | English |
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Pages (from-to) | 764-798 |
Number of pages | 35 |
Journal | ChemistrySelect |
Volume | 5 |
Issue number | 2 |
DOIs | |
Publication status | Published - Jan 16 2020 |
Externally published | Yes |
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