Please use this identifier to cite or link to this item:
https://olympias.lib.uoi.gr/jspui/handle/123456789/9988Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Adam, W. | en |
| dc.contributor.author | Gogonas, E. P. | en |
| dc.contributor.author | Hadjiarapoglou, L. P. | en |
| dc.date.accessioned | 2015-11-24T16:53:13Z | - |
| dc.date.available | 2015-11-24T16:53:13Z | - |
| dc.identifier.issn | 1434-193X | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9988 | - |
| dc.rights | Default Licence | - |
| dc.subject | insertions | en |
| dc.subject | rhodium | en |
| dc.subject | ylides | en |
| dc.subject | catalyzed intramolecular cyclopropanations | en |
| dc.subject | polyvalent iodine compounds | en |
| dc.subject | iodonium ylides | en |
| dc.subject | phenyliodonium ylides | en |
| dc.subject | ch-insertions | en |
| dc.subject | cycloaddition | en |
| dc.subject | decomposition | en |
| dc.subject | chemistry | en |
| dc.title | Bis(sulfonyl)methyl insertion into alkenyl versus phenyl carbon-hydrogen bonds in the reaction of bis(sulfonyl)iodonium ylides with highly phenylated ethylenes | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.secondary | <Go to ISI>://000181724600016 | - |
| heal.identifier.secondary | https://docs.google.com/file/d/0BxfLht5wJUEIYTEwMDk4N2MtZmQ3My00OWMxLWJlZWMtZjIxYzFjNjRkMTYy/edit?hl=en | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.publicationDate | 2003 | - |
| heal.abstract | The reaction of bis(sulfonyl)iodonium ylides alpha-gamma with triphenylethylene (2a) and tetraphenylethylene (2b) affords insertion products into the alkenyl and phenyl carbon-hydrogen bonds of the substrate. A mechanistically perplexing feature is the diversity displayed in the reactivity pattern of the bis(sulfonyl)iodonium ylides in their reaction with the phenylated alkenes. | en |
| heal.journalName | European Journal of Organic 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 | |
|---|---|---|---|---|
| Hadjiarapoglou-2003-Bis(sulfonyl)methyl insertion.pdf | 104.05 kB | Adobe PDF | View/Open Request a copy |
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