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Starting from 4-nitropyrazole, eight mesoionic pyrazolium-4-aminides were prepared by a six-step reaction sequence. The deprotonation of 1,2-disubstituted 4-amido-1H-pyrazolium salts by an anion exchange resin in its hydroxide form is the final step
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaae39d4e33a88002f34c1bee1d2f982
https://publica.fraunhofer.de/handle/publica/429390
https://publica.fraunhofer.de/handle/publica/429390
Autor:
Jan C. Namyslo, Kai Hillrichs, Olivia Doppleb, Nils L. Ahlburg, Andreas Schmidt, Eike G. Hübner
Publikováno v:
HETEROCYCLES. 96:1203
Publikováno v:
Tetrahedron. 71(2):276
N-Heterocyclic carbenes of indazole (indazol-3-ylidenes), which are substituted at N1 with aromatics were generated in situ from the corresponding indazolium salts. At 60 °C the indazol-3-ylidenes underwent a ring-opening under N–N bond cleavage t