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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sakhuja, Rajeev | - |
| dc.date.accessioned | 2021-11-11T10:59:10Z | - |
| dc.date.available | 2021-11-11T10:59:10Z | - |
| dc.date.issued | 2017-09-26 | - |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1002/asia.201701274 | - |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3356 | - |
| dc.description.abstract | Two efficient iodine-mediated strategies, which are economical and one-pot, are described to access bis(imidazo[1,2-a]pyridin-3-yl)sulfanes and bis(imidazo[1,2-a]pyridin-3-yl)disulfanes in chloroform and acetic acid, respectively, by a direct oxidative homocoupling of imidazo-heterocycles using inexpensive sodium sulfide as a sulfur source. These strategies are scalable, and an array of substrates delivered their corresponding stable sulfur-bridged imidazo-heterocycles in excellent yields. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Solvent-Driven | en_US |
| dc.subject | Synthesis of Bis(imidazo[1,2-a]pyridin-3-yl) | en_US |
| dc.subject | Disulfanes | 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: | Department of Chemistry | |
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