Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/22549Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sudini, Ravinder R | - |
| dc.contributor.author | Khire, Uday R | - |
| dc.contributor.author | Pandey, Rajesh K | - |
| dc.contributor.author | Kumar, Pradeep | - |
| dc.date.accessioned | 2013-10-23T08:39:05Z | - |
| dc.date.available | 2013-10-23T08:39:05Z | - |
| dc.date.issued | 2000-10 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/22549 | - |
| dc.description | 738-745 | en_US |
| dc.description.abstract | The synthesis of a variety of spirodiones 7,12 related to fredericamycin A 1 has been reported. The preparation of DielsA-lder adducts employing the nonfunctionalised and functionalised isobenzofurans 13, 14 as dienes and spirodiones 7, 12 as dienophiles has been described. The subsequent acid induced rearrangement of Diels-Alder adducts 15, 17, 19, 21 leads to the formation of spiro compounds 16, 18, 20, 22 related to fredericamycin A. | 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(10) [October 2000] | en_US |
| dc.title | Diels-Alder approach for the synthesis of spiro compounds related to Fredericamycin A | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.39B(10) [October 2000] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 39B(10) 738-745.pdf | 1.81 MB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.