D. N. Tomilin, L. N. Sobenina, M. D. Gotsko, I. A. Ushakov, B. A. Trofimov, “Reaction of 1-(het)aryl-3-bromoprop-2-ynones with furans in solid metal oxides or salts: cross-coupling or cycloaddition?”, Mendeleev Commun., 28:1 (2018), 20

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Mendeleev Communications, 2018, Volume 28, Issue 1, Pages 20–21
DOI: https://doi.org/10.1016/j.mencom.2018.01.004 (Mi mendc1648)

This article is cited in 2 scientific papers (total in 2 papers)

Communications

Reaction of 1-(het)aryl-3-bromoprop-2-ynones with furans in solid metal oxides or salts: cross-coupling or cycloaddition?

D. N. Tomilin, L. N. Sobenina, M. D. Gotsko, I. A. Ushakov, B. A. Trofimov

A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation

Full-text PDF (207 kB) Citations (2)

DOI: https://doi.org/10.1016/j.mencom.2018.01.004

Graphic abstract: Reaction of 1-(het)aryl-3-bromoprop-2-ynones with furans in solid metal oxides or salts: cross-coupling or cycloaddition?

Abstract: 1-(Het)aryl-3-bromoprop-2-ynones react with 2-(2-furyl)pyrrole in the Al₂O₃ or K₂CO₃ dispersion (room temperature, 1 h) to afford the cross-coupling products either at the furan or pyrrole rings. Furan and 2-methylfuran with 3-bromo-1-phenylprop-2-ynone under the same conditions give the Diels–Alder cycloadducts, while furan-2-carbaldehyde andits acetals are inactive.

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Document Type: Article

Language: English

Citation: D. N. Tomilin, L. N. Sobenina, M. D. Gotsko, I. A. Ushakov, B. A. Trofimov, “Reaction of 1-(het)aryl-3-bromoprop-2-ynones with furans in solid metal oxides or salts: cross-coupling or cycloaddition?”, Mendeleev Commun., 28:1 (2018), 20–21

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https://www.mathnet.ru/eng/mendc1648

https://www.mathnet.ru/eng/mendc/v28/i1/p20

This publication is cited in the following 2 articles:

Citing articles in Google Scholar: Russian citations, English citations
Related articles in Google Scholar: Russian articles, English articles

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