6569-17-1Relevant articles and documents
The rearrangements of α-imino-thioaldehydes into dihydro-1,3-thiazoles
Arnaud,Pelloux-Leon,Ripoll,Vallee
, p. 8389 - 8392 (1994)
α-Imino-thioaldehydes were generated by retro-Diels-Alder reaction under nash vacuum thermolysis conditions. They were found to be unstable and cyclized to 2,3-dihydro-1.3-thiazoles. This cyclization was investigated by ab initio calculations.
NEW REACTIONS WITH THIOALDEHYDES AND THIENIUM CATIONS
Arnaud, Roger,Chavant, Pierre-Yves,Hagoug, Fatiha,Pelloux-Leon, Nadia,Ripoll, Jean-Louis,Vallee, Yannick
, p. 319 - 320 (2007/10/02)
i) When generated under FVT conditions α-imino-thioaldehydes undergo a cyclization to dihydro-1,3-thiazoles. ii) Thienium cations, generated during a Pummerer reaction, can be trapped with dienes.