Rh-II-catalyzed thermal cyclopropanations of a phenyliodonium bis(carbomethoxy)methylide with alkenes and dienes
| dc.contributor.author | Georgakopoulou, G. | en |
| dc.contributor.author | Kalogiros, C. | en |
| dc.contributor.author | Hadjiarapoglou, L. P. | en |
| dc.date.accessioned | 2015-11-24T16:46:31Z | |
| dc.date.available | 2015-11-24T16:46:31Z | |
| dc.identifier.issn | 0936-5214 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9079 | |
| dc.rights | Default Licence | - |
| dc.subject | hypervalent iodine | en |
| dc.subject | ylide | en |
| dc.subject | rh-catalysis | en |
| dc.subject | alkene | en |
| dc.subject | 1,3-diene | en |
| dc.subject | cyclopropane | en |
| dc.subject | iodonium ylides | en |
| dc.subject | intramolecular cyclopropanation | en |
| dc.subject | <3+2>-cycloaddition reactions | en |
| dc.subject | carbenoid reactions | en |
| dc.title | Rh-II-catalyzed thermal cyclopropanations of a phenyliodonium bis(carbomethoxy)methylide with alkenes and dienes | en |
| heal.abstract | Iodonium ylide 2, derived from dimethyl malonate, undergoes facile thermal cycloaddition with alkenes and dienes catalyzed with Rh-2(OAc)(4) to form the corresponding cyclopropanedicarboxylates and vinylcyclopropanedicarboxylates, respectively, in excellent yields. | en |
| heal.access | campus | - |
| heal.fullTextAvailability | TRUE | - |
| heal.identifier.secondary | <Go to ISI>://000172596400005 | - |
| heal.identifier.secondary | https://docs.google.com/file/d/0BxfLht5wJUEIOTYyODUzMWYtMjM4NS00MWYxLWI4ZmEtYjRiNzUyOWZiMTk1/edit?hl=en&pli=1 | - |
| heal.journalName | Synlett | en |
| heal.journalType | peer reviewed | - |
| heal.language | en | - |
| heal.publicationDate | 2001 | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.type | journalArticle | - |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.type.en | Journal article | en |
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