116246-84-5Relevant academic research and scientific papers
Synthesis and 125Te NMR spectroscopy of α-tellurocarbonyl compounds and derivatives
Silks III,Odom,Dunlap
, p. 1105 - 1119 (2007/10/02)
The reaction of lithium alkyl-, alkenyl-, alkynyl-, and aryl tellurolates with α-bromocarbonyl compounds in anhydrous tetrahydrofuran gives the title compounds in yields ranging from 55-92%. The 125Te NMR chemical shift range for these compound
Synthesis of α-Phenyltelluro Carbonyl Compounds
Hiiro, Tomoki,Kambe, Nobuaki,Ogawa, Akiya,Miyoshi, Noritaka,Murai, Shinji,Sonoda, Noboru
, p. 1096 - 1097 (2007/10/02)
Several new α-phenyltelluro carbonyl compounds have been synthesized by the reaction of benzenetellurenyl iodide with lithium enolates derived from ketones, esters, and an amide in tetrahydrofuran at -78 deg C.
