Abstract:
The reaction of [(diacetoxy)iodo]benzene with furazan dicarboxylic acid was accompanied by a novel decarboxylative ring-cleavage reaction; the cyanogen N-oxide, reactive intermediate generated in the process, was dimerised or trapped by a dipolarophile.
Document Type:
Article
Language: English
Citation:
A. B. Sheremetev, S. M. Konkina, “Novel reaction of [bis(acyloxy)iodo]arenes”, Mendeleev Commun., 13:6 (2003), 277–278
Linking options:
https://www.mathnet.ru/eng/mendc4061
https://www.mathnet.ru/eng/mendc/v13/i6/p277
This publication is cited in the following 7 articles:
Viktor V. Zhdankin, Patai's Chemistry of Functional Groups, 2018, 1
Akira Yoshimura, Viktor V. Zhdankin, “Advances in Synthetic Applications of Hypervalent Iodine Compounds”, Chem. Rev., 116:5 (2016), 3328
Leonid L. Fershtat, Margarita A. Epishina, Alexander S. Kulikov, Igor V. Ovchinnikov, Ivan V. Ananyev, Nina N. Makhova, “An efficient access to (1H-tetrazol-5-yl)furoxan ammonium salts via a two-step dehydration/[3+2]-cycloaddition strategy”, Tetrahedron, 71:38 (2015), 6764
Leonid L. Fershtat, Ivan V. Ananyev, Nina N. Makhova, “Efficient assembly of mono- and bis(1,2,4-oxadiazol-3-yl)furoxan scaffolds via tandem reactions of furoxanylamidoximes”, RSC Adv., 5:58 (2015), 47248
Hypervalent Iodine Chemistry, 2013, 21
Viktor V. Zhdankin, Peter J. Stang, “Chemistry of Polyvalent Iodine”, Chem. Rev., 108:12 (2008), 5299
Aleksei B. Sheremetev, Svetlana M. Konkina, “Novel Reaction of [Bis(acyloxy)iodo]arenes.”, ChemInform, 35:19 (2004)
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