The one-pot reaction of sterically hindered hydrazones with tellurium dichloride or tellurium tetrahalide in the presence of triethylamine in benzene afforded Δ3-1,3,4-telluradiazolines 1, a novel heterocycle, via 1,3-dipolar cycloaddition of telluroketones and diazo compounds, both generated in situ. The molecular structure of 1a was established by X-ray crystallographic analysis. The photolysis of
Synthesis of Δ<sup>3</sup>-1,3,4-Telluradiazolines, a Novel Tellurium-Containing Heterocycle
作者:Renji Okazaki、Mao Minoura、Takayuki Kawashima
DOI:10.1246/cl.1993.1047
日期:1993.6
Reaction of sterically hindered hydrazones with tellurium dichloride in the presence of triethylamine in benzene afforded Δ3-1,3,4-telluradiazolines, a novel heterocycle, probably via 1,3-dipolar cycloaddition of telluroketones with diazo compounds, both generated in situ.
The First Isolation of a Telluroketone and Its Reversible Dimerization
作者:Mao Minoura、Takayuki Kawashima、Renji Okazaki*
DOI:10.1016/s0040-4039(97)00377-8
日期:1997.4
The solid-state thermolysis of a sterically hindered Delta(3)-1,3,4-telluradiazoline 2 afforded products resulting from intermediary tellone 1 and diazo compound 8 formed by retrocyclization, whereas the flash vacuum thermolysis of 2 led to isolation of tellone 1 as green needles. The spontaneous dimerization of 1 thus obtained occurred in the solid state to give the corresponding 1,3-ditelluretane 10, which underwent the thermal cycloreversion in solution to regenerate pure tellone 1. (C) 1997 Elsevier Science Ltd.