Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/3875Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Baskar, G | - |
| dc.contributor.author | Gopalakrishnan, M | - |
| dc.contributor.author | Jabaraj, J Winfred | - |
| dc.date.accessioned | 2009-04-17T04:26:55Z | - |
| dc.date.available | 2009-04-17T04:26:55Z | - |
| dc.date.issued | 2009-04 | - |
| dc.identifier.issn | 0376-4699 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/3875 | - |
| dc.description | 580-584 | en_US |
| dc.description.abstract | Analysis of the spectral data (1H NMR and13C NMR) indicates that out of ten N-hydroxypiperidin-4-one oximes 3a-j, the compounds 3b and 3c exist predominantly in chair conformation with the aryl and alkyl substituents in the equatorial positions, whereas the compounds 3d-j exist in boat conformation. The introduction of an oxime group at C-4 causes a flattening of the ring about C(5)-C(6) bond. The NOESY spectrum (Nuclear Overhauser effect) recorded for the compound 3d further supports the assigned boat conformation. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | IJC-B Vol.48B(04) [April 2009] | en_US |
| dc.subject | 1H NMR | en_US |
| dc.subject | en_US | |
| dc.subject | NOESY | en_US |
| dc.subject | conformation and N-hydroxypiperidone oximes | en_US |
| dc.title | Conformational analysis of some N-hydroxypiperidin-4-one oximes | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.48B(04) [April 2009] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 48B(4) 580-584.pdf | 78.2 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.