Izotiocijanat — разлика између измена

U ovoj sintezi<ref>{{ cite journal | author1 = Ortega-Alfaro, M. C. | author2 = López-Cortés, J. G. | author3 = Sánchez, H. R. | author4 = Toscano, R. A. | author5 = Carrillo, G. P. | author6 = Álvarez-Toledano, C. | title = Improved approaches in the synthesis of new 2-(1, 3-thiazolidin-2Z-ylidene)acetophenones | journal = Arkivoc | year = 2005 | volume = 2005 | issue = 6 | pages = 356–365 | url = http://www.arkat-usa.org/ark/journal/2005/I06_Juaristi/1528/EJ-1528C.asp | access-date = 07. 10. 2013 | archive-url = https://web.archive.org/web/20060426193809/http://www.arkat-usa.org/ark/journal/2005/I06_Juaristi/1528/EJ-1528C.asp | archive-date = 26. 04. 2006 | dead-url -status= yesdead | df = }}</ref> ultimatni reakcioni produkt je [[tiazolidin]]. Reakcija je [[stereoselektivnost|stereosektivna]], te se formira samo [[Geometrijski izomerizam|-{Z}--izomer]].