Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sandra Kaul"'
Autor:
Viktor A. Zapol’skii, Sandra Kaul, Bianka Karge, Mark Brönstrup, Mimoza Gjikaj, Dieter E. Kaufmann
Publikováno v:
Molecules, Vol 28, Iss 6, p 2479 (2023)
The reaction of mercaptoacetic acid esters with pentachloro-2-nitro-1,3-butadiene provides the appropriate precursors for the synthesis of 2,3,4-trisubstituted benzo[h]quinolines. These heterocycles are easily accessible via a single-step reaction wi
Externí odkaz:
https://doaj.org/article/de935e9722e242e4969013b4e10af1cf
Publikováno v:
Zeitschrift für Naturforschung B. 69:605-614
3-Methylindole reacts with pyridines in the presence of NBS to give indol-2-yl-pyridinium salts which were converted into their ylides by an anion exchange resin in its hydroxide form. Indol-3- amine was subjected to a nucleophilic ring transformatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd1f391856900fd2d721b03ca207f140
https://doi.org/10.5560/znb.2014-3324
https://doi.org/10.5560/znb.2014-3324
Autor:
Thomas Wirth, Sandra Kaul, Robert Alun Saunders, Alastair Baker, Gareth J. S. Evans, Michael Graz
Publikováno v:
Journal of Flow Chemistry. 3:118-121
Using mild conditions and short reaction times, symmetrical disulfides have been synthesized in flow chemistry using phase transfer catalysts to facilitate the substitution of organohalides with disodium disulfide. Also, the synthesis of symmetrical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19fcec928120bccc4dcb52c64742b329
https://doi.org/10.1556/jfc-d-13-00013
https://doi.org/10.1556/jfc-d-13-00013