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Reaction of diazoalkanes with unsaturated compounds
Authors:Yu. V. Tomilov  G. P. Okonnishnikova  E. V. Shulishov  K. N. Shavrin  O. M. Nefedov
Affiliation:(1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913 Moscow, Russian Federation
Abstract:A THF solution of diazopropyne was obtained in 60% yield by the reaction of a 30% aqueous solution of methylamine withN,N′-dinitroso-N,N′-dipropargylterephthalodiamide. The reactions of diazopropyne with methyl acrylate and methyl methacrylate giving various ethynylpyrazolines as well as its CuCl-catalyzed decomposition in the presence of norbornene or norbornadiene yielding ethynylcyclopropanes were studied. The main products of catalytic deazotization of diazopropyne in the absence of unsaturated compounds are isomericE- andZ-hex-3-ene-1,5-diynes resulting from propargylene dimerization. For Part 12, see Ref. 1. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2278–2282, November, 1998.
Keywords:diazopropyne  3- or 5-ethynylpirazolines  ethynylcyclopropanes  1,3-dipolar cycloaddition  catalytic ethynylcyclopropanation  NMR spectra
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