Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/16572Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Nandanan, E | - |
| dc.contributor.author | Phukan, Prodeep | - |
| dc.contributor.author | Sudalai, A | - |
| dc.date.accessioned | 2013-03-29T11:13:15Z | - |
| dc.date.available | 2013-03-29T11:13:15Z | - |
| dc.date.issued | 1999-08 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16572 | - |
| dc.description | 893-896 | en_US |
| dc.description.abstract | The synthesis of optically active β-hydroxy acids 5a-c is achieved in four steps from their corresponding terminal olefins 1a-c by employing Sharpless asymmetric dihydroxylation. The regioselective ring opening of chiral cyclic sulfites 3a-c with cyanide ion, constitutes the key reaction, thus producing the hydroxy nitriles 4a-c. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.38B(08) [August 1999] | en_US |
| dc.title | An efficient method to chiral β-hydroxy acids: Synthesis of lipid-A side chain | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(08) [August 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(8) 893-896.pdf | 885.25 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.