Please use this identifier to cite or link to this item:
http://dspace.mediu.edu.my:8181/xmlui/handle/123456789/124421Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.creator | Dardonville, Christophe | - |
| dc.creator | Jimeno, M. Luisa | - |
| dc.creator | Alkorta, Ibon | - |
| dc.creator | Elguero, José | - |
| dc.date | 2004-04-08 | - |
| dc.date.accessioned | 2017-01-31T01:41:17Z | - |
| dc.date.available | 2017-01-31T01:41:17Z | - |
| dc.identifier | ARKIVOC 2004 (ii) 206-212 | - |
| dc.identifier.uri | http://dspace.mediu.edu.my:8181/xmlui/handle/123456789/124421 | - |
| dc.description | When 5H-dibenz[b,f]azepine is dissolved in pure sulfuric acid it undergoes an oxidative dismutation into two acridine derivatives: 9-formylacridine and 9,9'-ethene-1,2-diyl-bis-acridine. | - |
| dc.description | DGI/MCyT of Spain (project BQU-2000-0645), European Community Marie Curie individual Fellowship (program: “Improving Human Research Potential and the Socio-economic Knowledge Base”, contract number: HMPF-CT-2001-01120), Spanish "Ministerio de Educación, Ciencia y Deportes" postdoctoral fellowship (SB2001-0174). | - |
| dc.description | Peer reviewed | - |
| dc.language | eng | - |
| dc.publisher | Arkat USA | - |
| dc.rights | openAccess | - |
| dc.subject | Azepine | - |
| dc.subject | Acridine | - |
| dc.subject | Dismutation | - |
| dc.subject | Rearrangement | - |
| dc.subject | NMR | - |
| dc.title | The behavior of 5H-dibenz[b,f]azepine dissolved in sulfuric acid | - |
| dc.type | Artículo | - |
| Appears in Collections: | Digital Csic | |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.