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http://hdl.handle.net/123456789/1688Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mandal, S.K. | - |
| dc.date.accessioned | 2020-11-17T09:31:47Z | - |
| dc.date.available | 2020-11-17T09:31:47Z | - |
| dc.date.issued | 2017 | - |
| dc.identifier.citation | Chemistry - An Asian Journal, 12 (23) | en_US |
| dc.identifier.other | 10.1002/asia.201701274 | - |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/full/10.1002/asia.201701274 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/1688 | - |
| dc.description | Only IISERM authors are available in the record. | - |
| dc.description.abstract | Twoefficient iodine-mediated strategies, which are economical and one-pot,are described to access bis(imi- dazo[1,2-a]pyridin-3-yl)sulfanes and bis(imidazo[1,2-a]pyri- din-3-yl)disulfanes in chloroform and acetic acid, respectively, by adirect oxidative homocoupli ng of imidazo-heterocycles using inexpensive sodiumsulfide as asulfur source.These strategies are scalable, andanarray of substrates delivered their corresponding stable sulfur-bridged imidazo-heterocy- cles in excellent yields. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | Wiley | en_US |
| dc.subject | Twoefficient | en_US |
| dc.subject | Solvent‐Driven | en_US |
| dc.subject | Sulfur heterocycles | en_US |
| dc.title | Solvent-Driven Iodine-Mediated Oxidative Strategies for the Synthesis of Bis(imidazo[1,2-a]pyridin-3-yl)sulfanes and Disulfanes | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Research Articles | |
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| File | Description | Size | Format | |
|---|---|---|---|---|
| Need to add pdf.odt | 8.63 kB | OpenDocument Text | View/Open |
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