Regioselective and diastereoselective dimethyldioxirane epoxidation of substituted norbornenes and hexamethyl Dewar benzene
dc.contributor.author | Asouti, A. | en |
dc.contributor.author | Hadjiarapoglou, L. P. | en |
dc.date.accessioned | 2015-11-24T16:46:16Z | |
dc.date.available | 2015-11-24T16:46:16Z | |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/9052 | |
dc.rights | Default Licence | - |
dc.subject | dimethyldioxirane | en |
dc.subject | epoxidation | en |
dc.subject | diastereoselectivity | en |
dc.subject | regioselectivity | en |
dc.subject | substituted norbornenes | en |
dc.subject | catalytic asymmetric epoxidation | en |
dc.subject | ketone catalysts | en |
dc.subject | dioxiranes | en |
dc.subject | chemistry | en |
dc.subject | oxidation | en |
dc.subject | olefins | en |
dc.subject | design | en |
dc.title | Regioselective and diastereoselective dimethyldioxirane epoxidation of substituted norbornenes and hexamethyl Dewar benzene | en |
heal.abstract | Various substituted norbornenes, such as endo-dicyclopentadiene 1, exo-dicyclopentadiene 5, 5-methylenebicyclo[2.2.1]hept-2-ene 8 and hexamethyl Dewar benzene 10 were transformed into the corresponding mono- and bis-epoxides by epoxidation with dimethyldioxirane (as an acetone solution). (C) 2000 Elsevier Science Ltd. All rights reserved. | en |
heal.access | campus | - |
heal.fullTextAvailability | TRUE | - |
heal.identifier.secondary | <Go to ISI>://000084947700024 | - |
heal.identifier.secondary | https://docs.google.com/file/d/0BxfLht5wJUEIM2ZjMmRhNjAtY2EzZi00ODdjLWIyZWEtYzRiMzY1NzNjZTY2/edit?hl=en | - |
heal.journalName | Tetrahedron Lett | en |
heal.journalType | peer reviewed | - |
heal.language | en | - |
heal.publicationDate | 2000 | - |
heal.publisher | Pergamon-Elsevier | en |
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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