1327166-05-1Relevant academic research and scientific papers
Highly Diastereoselective and Irreversible Aldol Reactions of N -Sulfonylimidates
Bartrum, Hannah E.,Carret, Sébastien,Poisson, Jean-Fran?ois
, p. 3413 - 3419 (2016)
A mild method for the aldolization of N-sulfonylimidates was developed. The reaction proceeds in excellent diastereoselectivity to provide a range of useful β-hydroxyimidates in high yield. The innate reversibility of the reaction is suppressed by the use of a titanium complex as a Lewis acid.
Highly controlling selectivity of copper(I)-catalyzed azide/alkyne cycloaddition (CuAAC) between sulfonyl azids and normal alkynes or propynoates
Liu, Yantao,Wang, Xinyan,Xu, Jimin,Zhang, Qun,Zhao, Yi,Hu, Yuefei
scheme or table, p. 6294 - 6299 (2011/09/19)
In this article, a combination of Cu(OAc)2·H 2O/2-aminophenol was developed as a highly efficient and controlling catalytic system for sulfonyl azids involved CuAAC. By using this catalytic system, sulfonyl azids reacted with normal
