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Trimethylsilylisothiocyanat (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Trimethylsilylisothiocyanat" in German language version.

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12doi.org
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doi.org

  • H.H. Anderson: Methyl silicon isothiocyanates. Molar refractions. In: J. Am. Chem. Soc. Band 69, Nr. 12, 1947, S. 3049–3051, doi:10.1021/ja01204a036.
  • R.H.C.N. Freitas: Trimethylsilyl Isothiocyanate (TMSNCS). In: Austr. J. Chem. Band 69, Nr. 8, 2016, S. 928–929, doi:10.1071/CH16057.
  • V. Golubev, F. Zubkov, M. Krasavin: A simple, three-component synthesis of 2-aminothiazoles using trimethylsilyl isothiocyanate. In: Tetrahedron Lett. Band 54, 2013, S. 4844–4847, doi:10.1016/j.tetlet.2013.06.102.
  • P.-Y. Renard, H. Schwebel, P. Vayron, E. Leclerc, S. Dias, C. Mioskowski: Optimized access to alkyl thiocyanates. In: Tetrahedron Lett. Band 42, Nr. 48, 2001, S. 8479–8481, doi:10.1016/S0040-4039(01)01846-9.
  • K. Nishiyama, M. Oba: Reactions of trimethylsilyl isothiocyanate with aldehydes and acetals. Synthesis of symmetrically and unsymmetrically isothiocyanato-substituted ethers. In: Bull. Chem. Soc. Jpn. Band 60, Nr. 6, 1987, S. 2289–2291, doi:10.1246/bcsj.60.2289.
  • D. Das, P. Sikdar, M. Bairaqi: Recent developments of 2-amino-thiazoles in medicinal chemistry. In: Eur. J. Med. Chem. Band 109, 2016, S. 89–98, doi:10.1016/j.ejmech.2015.12.022.
  • D.R. Guda, T. Wang, H.M. Cho, M.E. Lee: Trimethylsilyl isothiocyanate (TMSNCS): an efficient reagent for the one-pot synthesis of mercapto-1,2,4-triazoles. In: Tetrahedron Lett. Band 53, Nr. 39, 2012, S. 5238–5242, doi:10.1016/j.tetlet.2012.07.054.
  • R.M. Shaker: The chemistry of mercapto- and thione- substituted 1,2,4-triazoles and their utility in heterocyclic synthesis. In: ARKIVOC. Band 9, 2006, S. 59–112, doi:10.3998/ark.55550190.0007.904.
  • D.R. Guda, H.M. Cho, M.E. Lee: Mild and convenient one-pot synthesis of 2-amino-1,3,4-thiadiazoles using trimethylsilyl isothiocyanate (TMSNCS). In: RSC Adv. Band 3, 2013, S. 6813–6816, doi:10.1039/c3ra00159h.
  • G. Serban, O. Stanasel, E. Serban, S. Bota: 2-Amino-1,3,4-thiadiazoles as a potential scaffold for promising antimicrobial agents. In: Drug Des. Dev. Ther. Band 12, 2018, S. 1545–1566, doi:10.2147/DDDT.S155958h.
  • D.R. Guda, H.M. Cho, M.E. Lee: Mild and convenient one-pot synthesis of 2-amino-1,3,4-oxadiazoles promoted by trimethylsilyl isothiocyanate (TMSNCS). In: RSC Adv. Band 3, 2013, S. 7684–7687, doi:10.1039/c3ra41044g.
  • M. Bruno, R. Margarita, L. Parlanti, G. Piancatelli, M. Trifoni: Hypervalent iodine chemistry: Novel and direct thiocyanation of alkenes using [bis(acetoxy)iodo]benzene/trimethylsilyl isothiocyanate reagent combination. Synthesis of 1,2-dithiocyanates. In: Tetrahedron Lett. Band 39, Nr. 22, 1998, S. 3847–3848, doi:10.1016/S0040-4039(98)00629-7.

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  • Patent GB643941: Improvements in and relating to organo-silicon compounds. Angemeldet am 27. September 1950, veröffentlicht am 9. Juni 1948, Anmelder: The British Thomson-Houston Co. Ltd..‌
  • Patent GB643941: Improvements in and relating to organo-silicon compounds. Angemeldet am 9. Juni 1948, veröffentlicht am 27. September 1950, Anmelder: The British Thomson-Houston Co. Ltd..‌

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