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http://nopr.niscpr.res.in/handle/123456789/16626Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Shishoo, C J | - |
| dc.contributor.author | Jain, K S | - |
| dc.contributor.author | Jain, S R | - |
| dc.contributor.author | Shirsath, V S | - |
| dc.contributor.author | Ravikumar, T | - |
| dc.date.accessioned | 2013-03-29T19:16:29Z | - |
| dc.date.available | 2013-03-29T19:16:29Z | - |
| dc.date.issued | 1999-09 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16626 | - |
| dc.description | 1052-1065 | en_US |
| dc.description.abstract | The synthesis of a series of C(8) unsubstituled (11a-h), C(8) substituted (12a-e), 8-mercapto (13a-e) 1,3-diaryl-2- thioxanthines, as well as, 8-aza-1,3-diaryl-2-thioxanthines 14a-g, through precursors, 5,6-diamino-1,3-diaryl-2-thiouracils 10 has been reported. Recently, the synthesis of a novel series of 6-amino-1,3-diaryl-2-thiouracils 8 under the influence of dry HCI gas has been reported. 14.15. These compounds are converted to the requisite 5,6-diamino-1,3-diaryl-2-thiouracils 10 via reduction of an intermediate 5-nitroso-6-amino-1,3-diaryl-2-thiouracils 9. Cyclocondensation of 5,6-diamino-2- thiouracils 10 with appropriate one carbon donors afford the desired purines 11-13. | 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(09) [September 1999] | en_US |
| dc.title | Synthesis of purines and azapurines | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(09) [September 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(9) 1052-1065.pdf | 2.1 MB | Adobe PDF | View/Open |
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