D. V. Tsyganov, A. V. Samet, P. V. Dorovatovskii, V. N. Khrustalev, V. V. Semenov, “Arylglyoxal oximes as putative C-nucleophiles in eliminative nucleophilic substitution process”, Mendeleev Commun., 29:3 (2019), 296

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Mendeleev Communications, 2019, Volume 29, Issue 3, Pages 296–298
DOI: https://doi.org/10.1016/j.mencom.2019.05.018 (Mi mendc1501)

This article is cited in 3 scientific papers (total in 3 papers)

Communications

Arylglyoxal oximes as putative C-nucleophiles in eliminative nucleophilic substitution process

D. V. Tsyganov^a, A. V. Samet^a, P. V. Dorovatovskii^b, V. N. Khrustalev^bc, V. V. Semenov^a

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b National Research Centre 'Kurchatov Institute', Moscow, Russian Federation
^c Peoples Friendship University of Russia (RUDN University), Moscow, Russian Federation

Full-text PDF (287 kB) Citations (3) Supplementary materials

DOI: https://doi.org/10.1016/j.mencom.2019.05.018

Graphic abstract: Arylglyoxal oximes as putative C-nucleophiles in eliminative nucleophilic substitution process

Abstract: Reaction of arylglyoxal oximes ArCOCH=NOH (Ar=4-MeOC₆H₄, Ph) with 5-arylfurazanopyrazines proceeds as vicarious nucleophilic substitution of hydrogen in pyrazine ring with the elimination of hyponitrous acid, affording 5-(aroylmethylidene)-6-aryl-4H-furazano[3,4-b]pyrazines. Structure of the product was confirmed by X-ray diffraction.

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Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(327.4 Kb)

Citation: D. V. Tsyganov, A. V. Samet, P. V. Dorovatovskii, V. N. Khrustalev, V. V. Semenov, “Arylglyoxal oximes as putative C-nucleophiles in eliminative nucleophilic substitution process”, Mendeleev Commun., 29:3 (2019), 296–298

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https://www.mathnet.ru/eng/mendc1501

https://www.mathnet.ru/eng/mendc/v29/i3/p296

This publication is cited in the following 3 articles:

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