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., 28:2 (2018), 143

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Mendeleev Communications, 2018, Volume 28, Issue 2, Pages 143–144
DOI: https://doi.org/10.1016/j.mencom.2018.03.010 (Mi mendc1692)

This article is cited in 5 scientific papers (total 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

Full-text PDF (207 kB) Citations (5) Supplementary materials

DOI: https://doi.org/10.1016/j.mencom.2018.03.010

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

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.

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Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(361.4 Kb)

Citation: 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., 28:2 (2018), 143–144

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https://www.mathnet.ru/eng/mendc1692

https://www.mathnet.ru/eng/mendc/v28/i2/p143

This publication is cited in the following 5 articles:

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