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http://nopr.niscpr.res.in/handle/123456789/9098Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Agrawal, Pawan K | - |
| dc.date.accessioned | 2010-05-31T04:56:17Z | - |
| dc.date.available | 2010-05-31T04:56:17Z | - |
| dc.date.issued | 2005-05 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/9098 | - |
| dc.description | 1092-1094 | en_US |
| dc.description.abstract | A comparison of 1H NMR
chemical shifts for 25R and 25S spirostane-type steroidal
sapogenins and saponins suggest that orientation of 27-Me group has quite a
different influence on chemical shifts of the methylene protons occupying  -and  -positions, thus providing valuable
information about the establishment 25R-and 25S-stereochemistry
in these compounds. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl.7 C 07 J | en_US |
| dc.source | IJC-B Vol.44B(05) [May 2005] | en_US |
| dc.title | Determining ring-F configuration in spirostane-type steroidal sapogenins by 1H NMR | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.44B(05) [May 2005] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 44B(5) 1092-1094.pdf | 53.07 kB | Adobe PDF | View/Open |
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