Acyl iodides in organic synthesis: VII. Reactions with trialkyl(alkynyl)silanes,-germanes, and-stannanes
作者:M. G. Voronkov、A. A. Trukhina、N. N. Vlasova、R. G. Mirskov、O. G. Yarosh
DOI:10.1134/s1070428006010040
日期:2006.1
Reactions of acyl iodides (RCOI)-C-1 (R-1 = Me, Ph) with trialkyl(alkynyl)silanes, -germanes, and stannanes ((RC)-C-2=CMR33; M = Si, Ge, Sri) were studied. Acyl iodides reacted with the germanium and tin derivatives with cleavage of the M-C-sp bond and formation of the corresponding trialkyl(iodo)germanes and -stannanes RMI (M = Ge, Sri) and alkynyl ketones (RC)-C-1(O)C=CR2 and (RC)-C-1(O)C=CC(O)R-1. By contrast, the reaction of acetyl iodide with ethynyl(trimethyl)silane gave only a small amount of 1,2-diiodovinyl(trimethyl) silane as a result of iodine addition at the triple bond. Bis(trimethylsilyl)ethyne failed to react with acetyl iodide.