1978 巻 (1978) 5 号 p. 773-774
Decomposition of O-ethyl N-lithio-N-substituted thiocarbamates was accelerated by the addition of excess carbon disulfide or sulfur dioxide, and isothiocyanates were obtained in moderate yields even at room temperature.
O-Ethyl N-lithio-N-phenyl carbamate reacted with carbon disulfide to give phenyl isothiocyanate, but it reacted with sulfur dioxide to afford phenyl isocyanate as the trimer.