Synthesis and125Te NMR Spectroscopy of α-Tellurocarbonyl Compounds and Derivatives
摘要:
The reaction of lithium alkyl-, alkenyl-, alkynyl-, and aryl tellurolates with alpha-bromocarbonyl compounds in anhydrous tetrahydrofuran gives the title compounds in yields ranging from 55-92%. The Te-125 NMR chemical shift range for these compounds is 405-1024 ppm.
Synthesis and<sup>125</sup>Te NMR Spectroscopy of α-Tellurocarbonyl Compounds and Derivatives
作者:Louis A. Silks、Jerome D. Odom、R. Bruce Dunlap
DOI:10.1080/00397919108019802
日期:1991.4
The reaction of lithium alkyl-, alkenyl-, alkynyl-, and aryl tellurolates with alpha-bromocarbonyl compounds in anhydrous tetrahydrofuran gives the title compounds in yields ranging from 55-92%. The Te-125 NMR chemical shift range for these compounds is 405-1024 ppm.
Yamago, Shigeru; Ukai, Yuu; Matsumoto, Atsushi, Journal of the American Chemical Society, 2009, vol. 131, p. 2100 - 2101