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http://nopr.niscpr.res.in/handle/123456789/7360Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kumar, Rupesh | - |
| dc.contributor.author | Yusuf, Mohamad | - |
| dc.date.accessioned | 2010-02-15T10:05:22Z | - |
| dc.date.available | 2010-02-15T10:05:22Z | - |
| dc.date.issued | 2010-02 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/7360 | - |
| dc.description | 216-223 | en_US |
| dc.description.abstract | The photoirradiation of bischromones with trans-2-butenyl and 2-butynyl, has produced tetracyclic compounds and isomerized ethers as photoproducts. The formation of these photoproducts has been rationalized through H-abstraction by C=O group of the pyrone moiety. The chemical efficiency of the bischromone phototransformations is dictated by the nature of the intermediate spacer unit. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | IJC-B Vol.49B(02) [February 2010] | en_US |
| dc.subject | Photoisomerization | en_US |
| dc.subject | bischromones | en_US |
| dc.subject | chromophore | en_US |
| dc.subject | spacer unit | en_US |
| dc.subject | photocyclisation | en_US |
| dc.title | Synthesis and photochemical H-abstractions of some 2-thienyl/furyl-3-allyloxybischromones | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.49B(02) [February 2010] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 49B(2) 216-223.pdf | 192.45 kB | Adobe PDF | View/Open |
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H-abstraction by C=O group of the pyrone moiety. The chemical efficiency of the bischromone phototransformations is dictated by the nature of the intermediate spacer unit.