作者:L. I. Makarova、N. V. Sergienko、E. S. Trankina、A. A. Zhdanov、E. A. Ahmet"eva
DOI:10.1023/a:1022464802897
日期:——
The reactions of [(2-acetoxyetoxy)methyl]dimethylchlorosilane and 1-acetoxy-2-(dimethylchlorosilylmethoxy)benzene with the cage phenylcopper and phenylmanganese siloxanes leads to the cleavage of the M-O-Si bond to give metal chlorides and six-unit cyclosiloxanes with an acetoxy group in the organic substituent at the silicon atom. Methanolysis of these acetoxy derivatives does not affect the ring structure and affords the corresponding polyhydric alcohols.