Issue 11, 1989

F.t.i.r. study of ynamines and ketenimines produced by thermolysis of substituted isoxazolones

Abstract

Gas phase flow thermolysis of 3-methyl-4-(methylaminomethylidene)isoxazol-5(4H)-one yielded N-methylethynamine, HC[triple bond, length as m-dash]CNHMe, and N-methylketenimine, H2C[double bond, length as m-dash]C[double bond, length as m-dash]NMe, which were observed by f.t.i.r. spectroscopy. Attempts to detect the simplest ynamine, HC[triple bond, length as m-dash]CNH2, and ketenimine, H2C[double bond, length as m-dash]C[double bond, length as m-dash]NH, by an analogous route using the appropriately substituted isoxazolone were unsuccessful.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1989, 1841-1844

F.t.i.r. study of ynamines and ketenimines produced by thermolysis of substituted isoxazolones

J. August, K. Klemm, H. W. Kroto and D. R. M. Walton, J. Chem. Soc., Perkin Trans. 2, 1989, 1841 DOI: 10.1039/P29890001841

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