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DC Field | Value | Language |
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dc.contributor.author | Korakas, D. | en |
dc.contributor.author | Varvounis, G. | en |
dc.date.accessioned | 2015-11-24T16:50:56Z | - |
dc.date.available | 2015-11-24T16:50:56Z | - |
dc.identifier.issn | 0022-152X | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9662 | - |
dc.rights | Default Licence | - |
dc.title | The nitration of some 1-aryl(or benzyl)pyrroles | en |
heal.type | journalArticle | - |
heal.type.en | Journal article | en |
heal.type.el | Άρθρο Περιοδικού | el |
heal.identifier.secondary | <Go to ISI>://A1996VC21600015 | - |
heal.identifier.secondary | http://onlinelibrary.wiley.com/store/10.1002/jhet.5570330314/asset/5570330314_ftp.pdf?v=1&t=hmrggzop&s=595cdf08b802c8e6245140482b8b10bc67bf07e3 | - |
heal.language | en | - |
heal.access | campus | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
heal.publicationDate | 1996 | - |
heal.abstract | Nitration of 1-arylpyrroles la-e with acetyl nitrate, and 1-arylpyrroles, la-e and 1-(2-ethoxycarbonylbenzyl)pyrrole 4 with trifluoroacetyl nitrate gave the corresponding 2-nitro isomers 2a-e and 5, and 3-nitro isomers 3a-e and 6. 3-Nitropyrroles 3d and 3e were further nitrated with a mixture of nitric and sulfuric acids to give compounds 10, 11 and 12, respectively. Under the same conditions 1-(2-ethoxycarbonylbenzyl)-3-nitropyrrole 6 gave derivative 13. | en |
heal.publisher | Wiley-Blackwell | en |
heal.journalName | Journal of Heterocyclic Chemistry | en |
heal.journalType | peer reviewed | - |
heal.fullTextAvailability | TRUE | - |
Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ |
Files in This Item:
File | Description | Size | Format | |
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Korakas-1996-The nitration of som.pdf | 269.97 kB | Adobe PDF | View/Open Request a copy |
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