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http://nopr.niscpr.res.in/handle/123456789/9220Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Raghavan, Sadagopan | - |
| dc.contributor.author | Reddy, S Ramakrishna | - |
| dc.contributor.author | Rajitha, B | - |
| dc.date.accessioned | 2010-06-01T04:48:48Z | - |
| dc.date.available | 2010-06-01T04:48:48Z | - |
| dc.date.issued | 2005-11 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/9220 | - |
| dc.description | 2314-2321 | en_US |
| dc.description.abstract | A stereoselective synthesis of the enantiomer of the fatty acid chain of stevastelin is disclosed. The C4 methyl group is introduced regio- and stereoselectively via dimethylcuprate opening of epoxy alcohol while the C5 stereogenic center was introduced in a highly stereoselective fashion by Grignard reaction. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl.7 C 07 C, C 07 D // A 61 P 37/06 | en_US |
| dc.source | IJC-B Vol.44B(11) [November 2005] | en_US |
| dc.subject | Stereoselective synthesis | en_US |
| dc.subject | enantiomer | en_US |
| dc.subject | fatty acid | en_US |
| dc.subject | immunosuppressant | en_US |
| dc.subject | stevastelin | en_US |
| dc.subject | dimethylcuprate | en_US |
| dc.subject | epoxy alcohol | en_US |
| dc.subject | Grignard reaction | en_US |
| dc.title | Stereoselective synthesis of the enantiomer of the fatty acid component of the potent immunosuppressant, stevastelin | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.44B(11) [November 2005] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 44B(11) 2314-2321.pdf | 87.54 kB | Adobe PDF | View/Open |
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