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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kumar, Anil | - |
dc.date.accessioned | 2021-10-14T13:09:56Z | - |
dc.date.available | 2021-10-14T13:09:56Z | - |
dc.date.issued | 2020-09-15 | - |
dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202000996 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2812 | - |
dc.description.abstract | Synthesis of 3-(arylthio)imidazo[1,2-a]pyridin-2(3H)-ols has been achieved through a catalyst-free, one-pot reaction of 2-aminopyridinium bromides with sodium arenesulfinates. The tandem reaction involved intramolecular amidation followed by sulfenylation and afforded a wide range of 3-(arylthio)imidazo[1,2-a]pyridin-2(3H)-ols in moderate to excellent (33–85 %) yields. The method exhibited broad substrate scope with a wide range of functional group tolerance, and is amenable for gram-scale synthesis. | en_US |
dc.language.iso | en | en_US |
dc.publisher | EJOC | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Facile Synthesis | en_US |
dc.subject | Sodium Arenesulfinates | en_US |
dc.subject | 2-Aminopyridinium Bromides | en_US |
dc.title | A Facile Synthesis of 3-(Arylthio)imidazo[1,2-a]pyridin-2(3H)-ones from 2-Aminopyridinium Bromides and Sodium Arenesulfinates | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemistry |
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