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http://nopr.niscpr.res.in/handle/123456789/60106Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Singh, Sushma | - |
| dc.contributor.author | Devi, Poonam | - |
| dc.contributor.author | Pundeer, Rashmi | - |
| dc.contributor.author | Chaudhri, Vishwas | - |
| dc.date.accessioned | 2022-07-15T10:52:54Z | - |
| dc.date.available | 2022-07-15T10:52:54Z | - |
| dc.date.issued | 2022-07 | - |
| dc.identifier.issn | 2583-1321 (Online); 0019-5103 (Print) | - |
| dc.identifier.uri | http://nopr.niscpr.res.in/handle/123456789/60106 | - |
| dc.description | 776-779 | en_US |
| dc.description.abstract | In the present study, the utility of the hypervalent iodine(III) reagent, diacetoxyiodobenzene is extended for the efficient synthesis of variously substituted aryl cyanamides. The reaction presents efficient conversion of thioureas to cyanamides under the conditions of ambient temperature while stirring. This organoiodine(III) mediated method features easy isolation of the products and represents an excellent example illustrating thiophilic property of diacetoxyiodobenzene in the desulfurization of thioureas. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | NIScPR-CSIR, India | en_US |
| dc.source | IJC Vol.61(07) [July 2022] | en_US |
| dc.subject | Diacetoxyiodobenzene | en_US |
| dc.subject | Desulfurization | en_US |
| dc.subject | Thiophilicity | en_US |
| dc.subject | Aryl thiourea | en_US |
| dc.subject | Cyanamide | en_US |
| dc.title | Application of diacetoxyiodobenzene in the desulfurization of arylthioureas | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC Vol.61(07) [July 2022] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJC 61(7) 776-779.pdf | Main Article | 1.93 MB | Adobe PDF | View/Open |
| IJC 61(7) 776-779 Suppl. Data.pdf | Supplementary Data | 1.74 MB | Adobe PDF | View/Open |
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