Abstract:
Potassium cyanide reacts with 3-aryl-4-phenylsulfonylfuroxan/ furazan under mild conditions in DMF at room temperature in the presence of 18-crown-6 to afford 3-aryl-4-cyanofuroxan/ furazan in 45–50% yield.
Citation:
L. Annaratone, S. Guglielmo, K. Yu. Chegaev, “Direct introduction of cyano group on furoxan ring”, Mendeleev Commun., 27:6 (2017), 565–566
Linking options:
https://www.mathnet.ru/eng/mendc2060
https://www.mathnet.ru/eng/mendc/v27/i6/p565
This publication is cited in the following 6 articles:
Muhammad Abu Yousef, Ryosuke Matsubara, “Recent progress in synthesis and application of furoxan”, RSC Adv., 13:8 (2023), 5228
Ryosuke Matsubara, Chenlu Dong, Masahiko Hayashi, “Direct Arylation of Furoxan Using Potassium Aryltrifluoroborates”, HETEROCYCLES, 104:10 (2022), 1770
Fiorella Tomassini, “República y revolución: la crítica de Schlegel a Kant”, Isegoría, 2022, no. 66, e04
Nina N. Makhova, Leonid L. Fershtat, Comprehensive Heterocyclic Chemistry IV, 2022, 190
Nina N. Makhova, Leonid L. Fershtat, “Recent advances in the synthesis and functionalization of 1,2,5-oxadiazole 2-oxides”, Tetrahedron Letters, 59:24 (2018), 2317
B. V. Lyalin, V. L. Sigacheva, L. L. Fershtat, N. N. Makhova, V. A. Petrosyan, “Eco-friendly N–N coupling of aminofuroxans into azofuroxans under the action of electrogenerated hypohalites”, Mendeleev Commun., 28:5 (2018), 518–520
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