dc.contributor.author | Kumar, Anil | |
dc.contributor.author | Kumar, Dalip | |
dc.date.accessioned | 2021-10-14T13:11:10Z | |
dc.date.available | 2021-10-14T13:11:10Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01449c | |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2825 | |
dc.description.abstract | A simple and efficient strategy for the synthesis of imidazopyridine-fused indoles has been developed that involves one-pot sequential Knoevenagel condensation of readily available active methylene azoles with N-substituted-1H-indole-3-carboxaldehydes or N-substituted-1H-indole-2-carboxaldehydes followed by palladium-catalyzed intramolecular cross dehydrogenative coupling reaction. A series of 36 derivatives was prepared by using this strategy. The products were obtained in moderate to excellent (32–94%) yields and showed broad substrate scope with tolerance of various functional groups and was amiable for gram scale preparation without problems. | en_US |
dc.language.iso | en | en_US |
dc.publisher | RSC | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Synthesis | en_US |
dc.subject | Imidazopyridine-fused indoles | en_US |
dc.subject | Dehydrogenative coupling | en_US |
dc.title | Synthesis of imidazopyridine-fused indoles via one-pot sequential Knoevenagel condensation and cross dehydrogenative coupling | en_US |
dc.type | Article | en_US |
Files | Size | Format | View |
---|---|---|---|
There are no files associated with this item. |