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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hadjiarapoglou, L., | en |
dc.contributor.author | Varvoglis, A. | en |
dc.date.accessioned | 2015-11-24T16:46:09Z | - |
dc.date.available | 2015-11-24T16:46:09Z | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9035 | - |
dc.rights | Default Licence | - |
dc.title | Reactivity of phenyliodonium bis(aryl- or alkyl-sulphonyl)methylides towards thiobenzophenones | en |
heal.type | journalArticle | - |
heal.type.en | Journal article | en |
heal.type.el | Άρθρο Περιοδικού | el |
heal.identifier.primary | 10.1039/P19890000379 | - |
heal.identifier.secondary | http://pubs.rsc.org/en/Content/ArticleLanding/1989/P1/p19890000379#!divAbstract | - |
heal.language | en | - |
heal.access | campus | - |
heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
heal.publicationDate | 1989 | - |
heal.abstract | Thermal reactions of several phenyliodonium bis(aryl- or alkyl-sulphonyl)methylides with some thiobenzophenones are described. 4,4'-Dimethoxythiobenzophenone affords exclusively 2-arylsulphonyl-3-(4-methoxyphenyl)-6-methoxybenzo[b]thiophenes, whereas other thiobenzophenones may give also gem-bis(arylsulphonyl)thiiranes and in one case an unsaturated gem-disulphone. Some oxidation reactions of an ylide with various substrates occur either thermally or photochemically. | en |
heal.publisher | Royal Society of Chemistry | en |
heal.journalName | Journal of the Chemical Society, Perkin Transactions 1 | en |
heal.journalType | peer reviewed | - |
heal.fullTextAvailability | TRUE | - |
Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ |
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