2845-79-6Relevant academic research and scientific papers
Facile access to a variety of 2,5-biaryl-1,2,4-TRIAZOL-3-ones via regioselective N-arylation of triazolones
Park, Jiyeon,Chae, Junghyun
scheme or table, p. 2143 - 2146 (2010/11/16)
A selective synthetic method of the 2,5-biaryltriazolones has been developed via copper-catalyzed N-arylation reaction. Aryltriazolones, which were readily prepared from commercially available compounds, were N-arylated to 2,5-biaryltriazolones with high regioselectivity. This approach allows for access to a variety of 2,5-biaryl-1,2,4-trizol-3-ones in a simple and practical manner.
EXTENSION OF THE PINNER REACTION ON THE BASIS OF A NEW MODIFICATION
Magedov, I.V.,Usorov, M.I.,Smushkevich, Yu.I.
, p. 239 - 240 (2007/10/02)
A modification of the Pinner reaction of imidates was used to convert hydrazonates into acid hydrazides.
