324042-07-1Relevant academic research and scientific papers
Organo-catalytic synthesis of 1,3-thiazole derivatives
Khalaj, Arash,Khalaj, Mehdi
, p. 445 - 448 (2016/07/21)
An efficient synthesis of 1,3-thiazolidine derivatives has been achieved in which 2-pyridinecarboxaldehyde oxime was employed as a base catalyst to effect cyclisation between aziridines and CS2 in DMF at 40°C. A similar reaction between aziridi
Organocatalytic one-pot synthesis of functionalized 1,3-oxathiolanes and 1,3-thiazolidines
Ghazanfarpour-Darjani, Majid,Khodakarami, Alieh
, p. 829 - 835 (2016/03/23)
An efficient organocatalytic approach for the synthesis of 1,3-oxathiolanes and 1,3-thiazolidines is reported. In this methodology, conjugated base of nitromethane was employed as a potential organocatalyst to promote cyclization reaction between strained
Quickly FeCl3-catalyzed highly chemo- and stereo-selective [3 + 2] dipolar cycloaddition of aziridines with isothiocyanates
Gao, Lingfeng,Fu, Kai,Zheng, Gengxiu
, p. 47192 - 47195 (2016/06/06)
A FeCl3-catalyzed [3 + 2] cycloaddition reaction of aziridine with isothiocyanate was developed. The cycloaddition reaction was completed in two minutes with high chemoselectivity, stereoselectivity. 15 (tosylthiazolidin-2-ylidene)anilines were
Tributylphosphine-catalyzed cycloaddition of aziridines with carbon disulfide and isothiocyanate
Wu, Jing-Yu,Luo, Zhi-Bin,Dai, Li-Xin,Hou, Xue-Long
supporting information; experimental part, p. 9137 - 9139 (2009/04/11)
(Chemical Equation Presented) Aziridines underwent cyclization reaction with carbon disulfide and isothiocyanate in the presence of organophosphine to afford thiazolidinone derivatives in good to high yields. The mechanistic study revealed that organophosphine serves as a catalyst in the reaction.
