Stevens rearrangement of heterocyclic ammonium salts containing prop-2-yn-1-yl group
作者:A. Kh. Gyul’nazaryan、T. A. Sahakyan、G. T. Sargsyan、J. V. Grigoryan、G. M. Muradyan、A. M. Petrosyan、G. A. Panosyan
DOI:10.1134/s1070363216090140
日期:2016.9
Stevensrearrangement was studied of ammonium salts where piperidinium or morpholinium groups are linked to prop-2-yn-1-yl moiety and labile hydrogen atom functions (methoxycarbonylmethyl, phenacyl, cyanomethyl). In the case of phenacyl analog furan derivatives were formed, in other cases dienamines were the reaction products.