Iodine-Mediated Oxidation of Ynamides: A Facile Access to N-Monosubstituted α-Ketoamides and α-Ketoimides was written by Huang, Hai;He, Guangke;Zhu, Xiaolin;Jin, Xiaodong;Qiu, Shineng;Zhu, Hongjun. And the article was included in European Journal of Organic Chemistry in 2014.Related Products of 888329-88-2 This article mentions the following:
An efficient iodine-mediated oxidation reaction for ynamides has been developed to produce N-monosubstituted α-ketoamides and α-ketoimides. This oxidative method, which exhibits good functional group tolerance, was performed under mild conditions without a metal catalyst. In the experiment, the researchers used many compounds, for example, 3-(Phenylethynyl)oxazolidin-2-one (cas: 888329-88-2Related Products of 888329-88-2).
3-(Phenylethynyl)oxazolidin-2-one (cas: 888329-88-2) belongs to oxazolidine derivatives. Oxazolidines are well known as key portions of bioactive molecules or precursors of chiral molecules, as well as established chiral auxiliaries. Some reports highlighted again the effectiveness of oxazolidine-based compounds in driving the stereo- or diastereotopic outcome of chemical reactions.Related Products of 888329-88-2
Referemce:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem