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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kumar, Anil | - |
dc.contributor.author | Kumar, Dalip | - |
dc.date.accessioned | 2021-10-14T13:11:33Z | - |
dc.date.available | 2021-10-14T13:11:33Z | - |
dc.date.issued | 2021-11-25 | - |
dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/slct.201702025 | - |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2831 | - |
dc.description.abstract | A one-pot, atom-economical multicomponent reaction of 2-bromoindole-3-carbaldehydes, alkynes and ammonia was developed in the presence of copper catalyst for the synthesis of a series of 3-aryl-γ−carboline derivatives in good to high yields. The developed reaction involved formation of imine followed by copper-catalyzed directed Sonogashira coupling and intramolecular hydroamination sequence of reactions. This multicomponent approach features mild reaction conditions and good functional group tolerance to access variety of 3-aryl γ-carbolines. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Copper-Catalyzed | en_US |
dc.subject | Sonogashira Coupling | en_US |
dc.subject | Intramolecular Hydroamination | en_US |
dc.title | Copper-Catalyzed Tandem Imine Formation, Sonogashira Coupling and Intramolecular Hydroamination: A Facile Synthesis of 3-Aryl-γ−carbolines | en_US |
dc.type | Article | en_US |
Appears in Collections: | Department of Chemistry |
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