1582229-84-2Relevant academic research and scientific papers
Diastereoselective Electrophilic α-Hydroxyamination of N-tert-Butanesulfinyl Imidates
Ma, Peng-Ju,Liu, Hui,Lu, Chong-Dao,Xu, Yan-Jun
, p. 670 - 673 (2017)
Diastereoselective α-hydroxyamination of N-tert-butanesulfinyl imidates using nitrosoarenes is reported. A catalytic amount of base effectively promotes the hydroxyamination reaction of α-aryl-substituted imidates, and the resulting α-hydroxyamino imidates can be transformed into a range of synthetically useful intermediates.
