dc.contributor.author | Βαρβαρέσου, Αθανασία | el |
dc.contributor.author | Ιακώβου, Κρίτων | el |
dc.date.accessioned | 2015-04-29T16:06:59Z | |
dc.date.available | 2015-04-29T16:06:59Z | |
dc.date.issued | 2015-04-29 | |
dc.identifier.uri | http://hdl.handle.net/11400/9271 | |
dc.rights | Αναφορά Δημιουργού-Μη Εμπορική Χρήση-Όχι Παράγωγα Έργα 3.0 Ηνωμένες Πολιτείες | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
dc.source | http://onlinelibrary.wiley.com | en |
dc.source | http://onlinelibrary.wiley.com/doi/10.1002/jhet.5570390610/abstract | en |
dc.subject | Καλλυντικά | |
dc.subject | Χημικά παρασκευάσματα | |
dc.subject | Cosmetics | |
dc.subject | Chemical preparations | |
dc.title | Derivatives of 5-Oxy-pyrido[2,3-b]quinoxaline-9-carboxylic acid | en |
heal.type | journalArticle | |
heal.secondaryTitle | a tricyclic system useful for the synthesis of potential intercalators | en |
heal.classification | Aesthetics | |
heal.classification | Chemistry | |
heal.classification | Αισθητική | |
heal.classification | Χημεία | |
heal.classificationURI | http://id.loc.gov/authorities/subjects/sh85001441 | |
heal.classificationURI | http://id.loc.gov/authorities/subjects/sh85022986 | |
heal.classificationURI | **N/A**-Αισθητική | |
heal.classificationURI | **N/A**-Χημεία | |
heal.identifier.secondary | 10.1002/jhet.5570390610 | |
heal.language | en | |
heal.access | free | |
heal.recordProvider | Τεχνολογικό Εκπαιδευτικό Ίδρυμα Αθηνών. Σχολή Επαγγελμάτων Υγείας και Πρόνοιας. Τμήμα Αισθητικής και Κοσμητολογίας | el |
heal.publicationDate | 2009-03-11 | |
heal.bibliographicCitation | Varvaresou, A. and Iakovou, K. (2002) Derivatives of 5-Oxy-pyrido[2,3-b]quinoxaline-9-carboxylic acid: A tricyclic system useful for the synthesis of potential intercalators. "Journal of Heterocyclic Chemistry" 39 (6), p.1173-1176 | en |
heal.abstract | The synthesis of a new series of 5-oxy-pyrido[2,3-b]quinoxaline-9-carboxamides 4a-i and N1,N2-Bis(5-oxy-pyrido[2,3-b]quinoxaline-9-benzoyl)ethylenediamine (5) is reported starting from 2-chloro-3-nitropyri-dine. Fundamental steps of the synthetic pathway are i) preparation of 2-(3-nitro-pyridin-2-ylamino)benzoic acid (1) via copper-catalyzed condensation of 2-chloro-3-nitropyridine with o-anthranilic acid, ii) intramolecular cyclization of the acid 1 to 5-oxy-pyrido[2,3-b]quinoxaline-9-carboxylic acid (2b) upon treatment with concentrated sulfuric acid and oleum and iii) conversion of the acid 2 to the desired amides 4a-i and 5. Compounds 4a-i and 5 are oxygenated azaanalogs of phenazines, a wellknown series of intercalators with cytotoxic activity. | en |
heal.publisher | Wiley | en |
heal.journalName | Journal of Heterocyclic Chemistry | en |
heal.journalType | peer-reviewed | |
heal.fullTextAvailability | false |
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