Please use this identifier to cite or link to this item:
https://olympias.lib.uoi.gr/jspui/handle/123456789/8627Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Syrgiannis, Z. | en |
| dc.contributor.author | Elemes, Y. | en |
| dc.date.accessioned | 2015-11-24T16:42:58Z | - |
| dc.date.available | 2015-11-24T16:42:58Z | - |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | https://olympias.lib.uoi.gr/jspui/handle/123456789/8627 | - |
| dc.rights | Default Licence | - |
| dc.subject | ene reactions | en |
| dc.subject | triazolinediones | en |
| dc.subject | solvent addition | en |
| dc.subject | solvent isotope effects | en |
| dc.subject | triazolinedione ene reactions | en |
| dc.subject | transition-state structure | en |
| dc.subject | singlet oxygen | en |
| dc.subject | temperature-dependence | en |
| dc.subject | pyruvate decarboxylase | en |
| dc.subject | enzyme action | en |
| dc.subject | cis-alkenes | en |
| dc.subject | stereochemistry | en |
| dc.subject | nitrosoarene | en |
| dc.subject | mechanisms | en |
| dc.title | Nucleophile-solvent isotope effects between methanol isotopomers during the interception of aziridinium imide-'like' closed intermediates | en |
| heal.type | journalArticle | - |
| heal.type.en | Journal article | en |
| heal.type.el | Άρθρο Περιοδικού | el |
| heal.identifier.primary | DOI 10.1016/j.tetlet.2006.07.063 | - |
| heal.identifier.secondary | <Go to ISI>://000240670800028 | - |
| heal.identifier.secondary | http://ac.els-cdn.com/S0040403906014626/1-s2.0-S0040403906014626-main.pdf?_tid=4fa71d6cfbeed81cd0be49dc06df0088&acdnat=1333029111_b58fcb6eb6d7acff336cf6f848dbcb08 | - |
| heal.language | en | - |
| heal.access | campus | - |
| heal.recordProvider | Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας | el |
| heal.publicationDate | 2006 | - |
| heal.abstract | Deuterated methanol isotopomers were found to compete efficiently with normal methanol during the interception of an intermediate with structural characteristics of the aziridinium imide, formed in the reaction of N-phenyttriazolinedione with simple alkenes such as 2-methylpropene, 2-methyl-2-butene, and 2,3-dimethyl-2-butene. In general, a (trideuterio)methyl-group bearing methanol was found to add at the tertiary carbon atom of the intermediate more efficiently with regard to hydrogen isotopomeric methanol, and this result is explained in terms of the nucleophile-solvent isotope effect in an S(N)2-'Iike' transition state of solvent addition to the intermediate. (c) 2006 Elsevier Ltd. All rights reserved. | en |
| heal.publisher | Elsevier | en |
| heal.journalName | Tetrahedron Lett | 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 | |
|---|---|---|---|---|
| Syrgiannis-2006-Nucleophile-solvent.pdf | 119.17 kB | Adobe PDF | View/Open Request a copy |
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