E. Yu. Schmidt, I. V. Tatarinova, N. I. Protsuk, I. A. Ushakov, B. A. Trofimov, “Dioximes of 1,6-heptanediones from acetylene and ketones: only three atom-economic steps”, Mendeleev Commun., 2018, Volume 28, Issue 2,Pages <nobr>143

This article is cited in 5 papers

Communications

Dioximes of 1,6-heptanediones from acetylene and ketones: only three atom-economic steps

E. Yu. Schmidt^ab, I. V. Tatarinova^a, N. I. Protsuk^a, I. A. Ushakov^a, B. A. Trofimov^a

^a A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
^b Angarsk State Technical University, Angarsk, Russian Federation

Abstract: 2-Acetyl-3,4-dihydropyrans, synthesized from acetylene and ketones in two steps, react with hydroxylamine to afford 5-hydroxy-1,6-heptanedione dioximes (E,E-isomers) in 72–96% yields.

Language: English

DOI: 10.1016/j.mencom.2018.03.010

	*Supplementary materials:*
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