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http://nopr.niscpr.res.in/handle/123456789/6639Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Thenmozhiyal, J C | - |
| dc.contributor.author | Venkatraj, M | - |
| dc.contributor.author | Jeyaraman, R | - |
| dc.contributor.author | Ponnuswamy, S | - |
| dc.date.accessioned | 2009-11-18T07:48:27Z | - |
| dc.date.available | 2009-11-18T07:48:27Z | - |
| dc.date.issued | 2006-08 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/6639 | - |
| dc.description | 1887-1893 | en_US |
| dc.description.abstract | r-2,c-6-Diphenylpiperidin-4-ones 2-6 and r-2,c-6-diphenylpiperidine 7 are treated with DMD and the reaction is found to yield only the corresponding N-hydroxy derivatives 8-13. The preferred conformations of the N-hydroxy compounds 8-13 are analysed using the NMR spectra and semiempirical molecular orbital calculations. The N-hydroxy derivatives 8-13 are found to prefer distorted chair conformations. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int. Cl.8 C07D | en_US |
| dc.source | IJC-B Vol.45B(08) [August 2006] | en_US |
| dc.subject | Dimethyldioxirane | en_US |
| dc.subject | diphenylpiperidine | en_US |
| dc.subject | conformation | en_US |
| dc.subject | MO calculation | en_US |
| dc.title | Synthesis of N-hydroxy-r-2,c-6-diphenylpiperidines using DMD and their stereochemical studies by NMR spectra and semiempirical MO calculations | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.45B(08) [August 2006] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 45B(8) 1887-1893.pdf | 102.05 kB | Adobe PDF | View/Open |
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