Intramolecular radical substitution on the sulfur of thioester, sulfide, sulfoxide, and sulfone
作者:Masaru Tada、Hiroyuki Nakagiri
DOI:10.1016/s0040-4039(00)61011-0
日期:1992.10
Alkyl radicals having the sulfur functions such as thioester, sulfide, and sulfoxide at the γ-position gave five membered cyclic thiolactone, sulfide and sulfoxide, while sulfone did not react with the alkyl radical. The product expectad from the sulfuranyl radical intermediate, which can pseudo-rotate, was not obtained.