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http://nopr.niscpr.res.in/handle/123456789/6635Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Srikrishna, A | - |
| dc.contributor.author | Kumar, P Ravi | - |
| dc.contributor.author | Gharpure, S J | - |
| dc.date.accessioned | 2009-11-18T07:44:20Z | - |
| dc.date.available | 2009-11-18T07:44:20Z | - |
| dc.date.issued | 2006-08 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/6635 | - |
| dc.description | 1909-1919 | en_US |
| dc.description.abstract | A combination of intermolecular Michael addition followed by intramolecular Michael addition of an enone to methyl acrylate and an intramolecular rhodium carbenoid CH insertion reaction of a diazo ketone have been exploited for the construction of isotwistanes. It has been extended to racemic and enantiospecific synthesis of 2-pupukeanone. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int. Cl.8 C07C | en_US |
| dc.source | IJC-B Vol.45B(08) [August 2006] | en_US |
| dc.subject | Pupukeananes | en_US |
| dc.subject | marine sesquiterpenes | en_US |
| dc.subject | Michael-Michael reaction | en_US |
| dc.subject | rhodium carbenoid | en_US |
| dc.subject | intramolecular CH-insertion | en_US |
| dc.title | An enantiospecific synthesis of 2-pupukeanone | 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) 1909-1919.pdf | 173.09 kB | Adobe PDF | View/Open |
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