828923-12-2Relevant academic research and scientific papers
Interaction of N,N-dimethyl-hydrazonomethyl and α-hydroxyketone groups in hetaryl analogs of unsymmetrical benzoins
Ivonin,Lapandin,Shtamburg
, p. 1484 - 1493 (2007/10/03)
The reaction of phenylglyoxal hydrate with N,N-dimethylhydrazones of furfural and 1-methylpyrrole-2-carbaldehyde proceeds regioselectively at position 5 of the heterocycle. The hetaryl analogs of α-benzoins obtained are quantitatively isomerized into the
Mutual influence of (dimethylhydrazono)methyl groups and α-hydroxy ketone moieties in hetaryl analogues of unsymmetric benzoins
Ivonin, Sergey P.,Lapandin, Audrey V.,Anishchenko, Audrey A.,Shtamburg, Vasilii G.
, p. 4688 - 4693 (2007/10/03)
Reactions between phenylglyoxal hydrate and the N,N-dimethylhydrazones of furfural and pyrrole-2-carbaldehyde run regioselectively at the 5-position of the heterocycle. The resulting hetaryl analogues of α-benzoins quantitatively isomerize to β-compounds,
