화학공학소재연구정보센터
Chemistry Letters, Vol.34, No.12, 1674-1675, 2005
Deprotonation of aryl methanedithioate by lithium amides: Formation of lithium arylthio(thioxo)methanide having unique reactivity
Deprotonation of aryl methanedithioate 5 bearing a bowl-type bulky subsituent with lithium tetramethylpiperidide at low temperature gave organolithium species 9 which was in equilibrium with a dimeric species 10; 9 extruded C=S at higher temperatures, thus representing a new, convenient source of C=S.