Synthesis and relative stability of five- and six-membered S-functional derivatives of 1,3-thiasilacycloalkanes
作者:Elena N Suslova、Aleksandr I Albanov、Bagrat A Shainyan
DOI:10.1016/s0022-328x(03)00348-6
日期:2003.7
Oxidation, imidation, and S-methylation reactions of five- and six-membered 1,3-thiasilacycloalkanes have been examined under various conditions. The S-functional derivatives of 1,3-thiasilacycloalkanes undergo solvolytic SiC(S) bond cleavage in protic media. The ease of the ring opening depends on the S-functionality and on the ring size.
已经在各种条件下检查了五元和六元1,3-硫代硅烷基环烷烃的氧化,酰亚胺化和S-甲基化反应。在小号的1,3- thiasilacycloalkanes官能化衍生物进行溶剂化SiC(S)键断裂在质子介质。开环的难易程度取决于S功能和环的大小。