Uses
1-Phenyl-1-hexyne is an alkyne. Stereoselective hydrogenation of 1-phenyl-1-hexyne at 298K and atmospheric pressure of H
2 over Pd catalysts supported on mesostructured silica is reported.
Polymerization of 1-phenyl-1-hexyne by pentahalides of niobium and tanatalum has been reported.
Electrolytically induced, base-catalyzed isomerization of 1-phenyl-1-hexyne to 1-phenyl-1, 2-hexadiene in dimethylformamide containing tetra-
n-butylammonium perchlorate using glassy carbon rotating ring-disk electrode has been reported.
Synthesis Reference(s)
The Journal of Organic Chemistry, 44, p. 3444, 1979
DOI: 10.1021/jo01333a049
General Description
1-Phenyl-1-hexyne is an alkyne. Stereoselective hydrogenation of 1-phenyl-1-hexyne at 298K and atmospheric pressure of H
2 over Pd catalysts supported on mesostructured silica is reported. Polymerization of 1-phenyl-1-hexyne by pentahalides of niobium and tanatalum has been reported. Electrolytically induced, base-catalyzed isomerization of 1-phenyl-1-hexyne to 1-phenyl-1, 2-hexadiene in dimethylformamide containing tetra-
n-butylammonium perchlorate using glassy carbon rotating ring-disk electrode has been reported.
