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http://nopr.niscpr.res.in/handle/123456789/22488Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Hariprakasha, H K | - |
| dc.contributor.author | Shanker, P Sathya | - |
| dc.contributor.author | Rao, G S R Subba | - |
| dc.date.accessioned | 2013-10-23T04:12:21Z | - |
| dc.date.available | 2013-10-23T04:12:21Z | - |
| dc.date.issued | 2000-02 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/22488 | - |
| dc.description | 94-102 | en_US |
| dc.description.abstract | A novel method for the construction of tricyclo[5 .3.1.01,5]undecane and tricyclo[6.3 .1 .0 1,6]dodecane frame work has been developed. Thus the alcohols 6, 18, 21 and 29 undergo Lewis acid-catalysed rearrangement to the tricyclic ketones 5, 19, 22 and 30. Dehydrogenation of 22 to the enone 23 proves the synchronous anti-migration of the methanobridge during the skeletal rearrangement. Finally, one carbon homologation of the ketones 5 and 19 leads to the syntheses of 2-norcedrene 4 and some analogues of funebrene 20 and 30. | 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.39B(02) [February 2000] | en_US |
| dc.title | Synthesis based on cyclohexadienes: Part 301 — Syntheses of 2-nor-cedrene and some analogues of funebrene | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.39B(02) [February 2000] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 39B(2) 94-102.pdf | 2.12 MB | Adobe PDF | View/Open |
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