Please use this identifier to cite or link to this item:
http://nopr.niscair.res.in/handle/123456789/8983| Title: | Approaches to sesquiterpenes containing three contiguous quaternary carbon atoms. Synthesis of 3-methoxythapsene |
| Authors: | Srikrishna, A Ramachary, D B |
| Issue Date: | Apr-2005 |
| Publisher: | CSIR |
| IPC Code: | Int.Cl.7 C 07 C 13/10 |
| Abstract: | Synthetic approach to 3-alkoxythapsane, comprising of the carbon framework of a small group of sesquiterpenes containing three contiguous quaternary carbon atoms has been described. A combination of alkylation, orthoester Claisen rearrangement and intramolecular diazoketone cyclopropanation has been employed for the creation of the three requisite contiguous quaternary carbon atoms. |
| Page(s): | 751-761 |
| URI: | http://hdl.handle.net/123456789/8983 |
| ISSN: | 0975-0983(Online); 0376-4699(Print) |
| Appears in Collections: | IJC-B Vol.44B(04) [April 2005] |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 44B(4) 751-761.pdf | 132.39 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.