Synthesis and biological activity of organosilicon esters

…, TN Povarnitsyna, AF Goleneva, LG Mardanova…

Index: Lapkin, I. I.; Pidemskii, E. L.; Povarnitsyna, T. N.; Goleneva, A. F.; Mardanova, L. G.; Dvinskikh, V. V. Pharmaceutical Chemistry Journal, 1983 , vol. 17, # 7 p. 496 - 500 Khimiko-Farmatsevticheskii Zhurnal, 1983 , vol. 17, # 7 p. 817 - 822

Full Text: HTML

Citation Number: 1

Abstract

All of the compounds prepared were colorless liquids, poorly soluble in water and very soluble in organic solvents. Their structures were confirmed by elemental analysis and IR spectra, which showed bands in the 1738-1758 cm-Zlregion (C= O of ester carbonyl); compounds containing hydrogen bonded to silicon had absorption bands at 2115-2120 cm-I (Si--H)(for other compounds, this band was absent), and 1090-1110 cm-I (Si-O).