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Molecular Rearrangement of 9b-Hydroxy-1H-imidazo[4,5-c]quinoline-2,4-diones - A Convenient Pathway to Spiro-Linked Imidazolidine-Oxindole Derivatives
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SYSNO ASEP 0328963 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Molecular Rearrangement of 9b-Hydroxy-1H-imidazo[4,5-c]quinoline-2,4-diones - A Convenient Pathway to Spiro-Linked Imidazolidine-Oxindole Derivatives Title Molekulární přesmyk 9b-Hydroxy-1H-imidazo[4,5-c]quinoline-2,4-dionů – Konvenční cesta k spiro-navázaným imidazolidin-oxindol derivátům Author(s) Klásek, A. (CZ)
Lyčka, A. (CZ)
Mikšík, Ivan (FGU-C) RID, ORCID, SAI
Růžička, A. (CZ)Source Title Helvetica Chimica Acta - ISSN 0018-019X
Roč. 92, č. 4 (2009), s. 689-708Number of pages 20 s. Language eng - English Country CH - Switzerland Keywords spiro-oxindoles ; aminoquinolinediones Subject RIV CC - Organic Chemistry CEZ AV0Z50110509 - FGU-C (2005-2011) UT WOS 000265475700010 DOI 10.1002/hlca.200800338 Annotation The elaborated methods allow to prepare spiro-oxindoles from 3-aminoquinolinediones in good to very good yields. The molecular rearrangement of compounds is not only of theoretical importance but enables, through a simple procedure, a targeted preparation of new types of spiro-oxindoles suitable both for biological testing as well as for studying further transformations Workplace Institute of Physiology Contact Lucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400 Year of Publishing 2010
Number of the records: 1