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https://olympias.lib.uoi.gr/jspui/handle/123456789/8865Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Adam, W. | en |
| dc.contributor.author | Gogonas, E. P. | en |
| dc.contributor.author | Nyxas, L. A. | en |
| dc.contributor.author | Hadjiarapoglou, L. P. | en |
| dc.date.accessioned | 2015-11-24T16:45:00Z | - |
| dc.date.available | 2015-11-24T16:45:00Z | - |
| dc.identifier.issn | 0039-7881 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/8865 | - |
| dc.rights | Default Licence | - |
| dc.subject | iodonium ylide | en |
| dc.subject | chalcones | en |
| dc.subject | diastereoselectivity | en |
| dc.subject | regioselectivity | en |
| dc.subject | 1,2,3-trisubstituted indanes | en |
| dc.subject | alpha,beta-unsaturated ketones | en |
| dc.subject | rearrangement | en |
| dc.subject | sulfones | en |
| dc.subject | facile | en |
| dc.subject | epoxidation | en |
| dc.subject | alkenes | en |
| dc.subject | esters | en |
| dc.subject | ylides | en |
| dc.title | [3+2] cycloaddition of phenyliodonium bis(arylsulfonyl)methylides with alpha,beta-enones | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | DOI 10.1055/s-2007-990801 | - |
| heal.identifier.secondary | <Go to ISI>://000250719600019 | - |
| heal.identifier.secondary | https://www.thieme-connect.de/ejournals/pdf/synthesis/doi/10.1055/s-2007-990801.pdf | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.publicationDate | 2007 | - |
| heal.abstract | The [3+2] cycloaddition of phenyliodonium bis(arylsulfonyl)methylides to alpha,beta-enones affords exclusively trans,trans-configured 1-(arylsulfonyl)-2-aroyl-3-arylindanes. The initial electrophilic attack of the iodonium ylide on the alkenyl double bond of the chalcone, followed by cyclization of the dipolar species, and subsequent ejection of iodobenzene and sulfur dioxide, stereoselectively affords the indane cycloadduct. | en |
| heal.journalName | Synthesis-Stuttgart | 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 | |
|---|---|---|---|---|
| Adam-2007-[3+2] cycloaddition.pdf | 144.94 kB | Adobe PDF | View/Open Request a copy |
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