209797-40-0Relevant academic research and scientific papers
Reaction of organozinc halides with aryl isocyanates
Yang, Haoran,Huang, Danfeng,Wang, Ke-Hu,Xu, Changming,Niu, Teng,Hu, Yulai
supporting information, p. 2588 - 2593 (2013/03/28)
Reformatsky reagent, benzylzinc bromide or alkylzinc iodides react with aryl isocyanates directly to give corresponding N-substituted carbamates under mild reaction conditions. However, the reaction of allylzinc bromide or propargylzinc bromide with aryl isocyanates produces the corresponding N-substituted amides. The reactions provide alternative methods for the synthesis of N-substituted carbamates or amides.
The Synthesis of Butenamides and Thiobutenamide by an Organosamarium Reagent
Yu, Mingxin,Zhang, Yongmin,Qian, Cangtao
, p. 256 - 257 (2007/10/03)
An organosamarium reagent reacts with isocyanates (or isothiocyanate) to afford butenamides (or thiobutenamide) in THF.
