LRC Digital repo
DSpace preserves and enables easy and open access to all types of digital content including text, images, moving images, mpegs and data sets
Please use this identifier to cite or link to this item:
https://dspace.ctu.edu.vn/jspui/handle/123456789/46271Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Erfle, Silke | - |
| dc.contributor.author | Langer, Peter | - |
| dc.date.accessioned | 2021-03-10T08:30:37Z | - |
| dc.date.available | 2021-03-10T08:30:37Z | - |
| dc.date.issued | 2020 | - |
| dc.identifier.issn | 2525-2321 | - |
| dc.identifier.uri | https://dspace.ctu.edu.vn/jspui/handle/123456789/46271 | - |
| dc.description.abstract | The reaction of dimethyl 3,5-dioxopimelate, a readily available 1,3,5,7-tetracarbonyl compound, with benzyne resulted in formation of a highly functionalized naphthalene derivative which is formed by an unprecedentcd domino ‘insertion / aldol condensation’ reaction. | vi_VN |
| dc.language.iso | vi | vi_VN |
| dc.relation.ispartofseries | Vietnam Journal of Chemistry;No.06, Vol.58 .- P.841-843 | - |
| dc.subject | Naphthalene | vi_VN |
| dc.subject | Benzyne | vi_VN |
| dc.subject | Insertions | vi_VN |
| dc.subject | 1,3-dicarbonyl compounds | vi_VN |
| dc.subject | Doinino reaction | vi_VN |
| dc.title | Domino Reaction of Benzyne with Dimethyl 3,5-Dioxopimelate | vi_VN |
| dc.type | Article | vi_VN |
| Appears in Collections: | Vietnam Journal of Chemistry | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| _file_ Restricted Access | 722.51 kB | Adobe PDF | ||
| Your IP: 3.147.46.174 |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.