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Ionic liquids-assisted ring opening of three-membered heterocycles with thio- and seleno-silanes

Please always quote using this URN: urn:nbn:de:bvb:20-opus-290350
  • Ring opening reactions of strained heterocycles (epoxides, aziridines, thiiranes) by silyl chalcogenides, such as thiosilanes and selenosilanes, can be efficiently performed in a variety of ionic liquids, which can behave as reaction media and in some cases also as catalysts. This protocol enables an alternative access to β-functionalized sulfides and selenides under mild conditions.

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Metadaten
Author: Damiano Tanini, Tommaso Pecchi, Nikolai V. Ignat’ev, Antonella Capperucci
URN:urn:nbn:de:bvb:20-opus-290350
Document Type:Journal article
Faculties:Fakultät für Chemie und Pharmazie / Institut für Anorganische Chemie
Language:English
Parent Title (English):Catalysts
ISSN:2073-4344
Year of Completion:2022
Volume:12
Issue:10
Article Number:1259
Source:Catalysts (2022) 12:10, 1259. https://doi.org/10.3390/catal12101259
DOI:https://doi.org/10.3390/catal12101259
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
Tag:ionic liquids; ring opening reactions; selenolysis; silyl selenides; silyl sulfides; thiolysis
Release Date:2023/11/07
Date of first Publication:2022/10/17
Licence (German):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International