Abstract:
A new type of ring–chain tautomerism, which consists in the reversible conversion of γ-halobutyric acid dialkylamides into dialkyl(tetrahydro-2,2-furylidene)ammonium halides, was found.
Document Type:
Article
Language: English
Citation:
M. V. Zlokazov, A. V. Lozanova, V. V. Veselovsky, “New examples of ring–chain tautomeric conversions”, Mendeleev Commun., 13:6 (2003), 242–243
Linking options:
https://www.mathnet.ru/eng/mendc4043
https://www.mathnet.ru/eng/mendc/v13/i6/p242
This publication is cited in the following 7 articles:
Ramil' N. Khusnitdinov, Rail R. Gataullin, “Synthesis and properties of 4-acetyl- and 4-alkoxycarbonyl-3-iodohexahydrocyclopenta[b]indoles”, Chem Heterocycl Comp, 51:9 (2015), 814
Laura Guasch, Markus Sitzmann, Marc C. Nicklaus, “Enumeration of Ring–Chain Tautomers Based on SMIRKS Rules”, J. Chem. Inf. Model., 54:9 (2014), 2423
A. V. Lozanova, A. V. Stepanov, V. V. Veselovsky, “A study of tautomerism in N,N-dialkyl-4(5)-bromoalkanecarboxamides”, Russ Chem Bull, 59:6 (2010), 1237
M. V. Zlokazov, V. V. Veselovsky, “Unusual transformation of (1R,1′S,2S)-1-(3-diisopropylamino-3-oxopropyl)-2-(1-hydroxyethyl)cyclopropane in the course of the cyclopropylcarbinyl rearrangement”, Russ Chem Bull, 58:2 (2009), 322
A. V. Lozanova, T. M. Ugurchieva, V. V. Veselovsky, “Stereoselective synthesis of 2,4-disubstituted butanolides”, Russ Chem Bull, 56:1 (2007), 130
A. V. Lozanova, T. M. Ugurchieva, M. V. Zlokazov, A. V. Stepanov, V. V. Veselovsky, “Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide”, Mendeleev Commun., 16:1 (2006), 15–16
Mikhail V. Zlokazov, Antonina V. Lozanova, Vladimir V. Veselovsky, “New Examples of Ring‐Chain Tautomeric Conversions.”, ChemInform, 35:17 (2004)
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