Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3887
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dc.contributor.authorKeri, R S-
dc.contributor.authorPatil, M-
dc.contributor.authorBudagumpi, S-
dc.contributor.authorSasidhar, B S-
dc.date.accessioned2021-11-18T12:09:00Z-
dc.date.available2021-11-18T12:09:00Z-
dc.date.issued2021-09-
dc.identifier.citationApplied Organometallic Chemistry; 35(9): e6316.en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/aoc.6316-
dc.identifier.urihttp://hdl.handle.net/123456789/3887-
dc.description.abstractThe design and application of environmentally friendly catalysts to reduce the number of toxic wastes are critical for improving the chemical synthetic protocols. A simple, mild, efficient, and eco-friendly method was developed for the synthesis of a series of Betti bases, 1-(α-aminoalkyl)naphthols, via a one-pot, multi-component reaction from aldehydes, β-naphthol and secondary amines in the presence of H-ZSM-5 as a catalyst at room temperature. The key advantages of the new protocol are environmentally friendly as it offers some interesting promising reaction prerequisites such as mild condition, safe, minimal waste, low cost, short reaction time and atom efficiency, easy workup, high to excellent yields, and possessing excellent functional group tolerance to synthesize structurally diverse derivatives. The catalyst is readily recovered by simple decantation and recycled several times with no significant loss in the catalytic activity.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.titleAn efficient, multicomponent synthesis of aminoalkylnaphthols via Betti reaction using ZSM‐5 as a recoverable and reusable catalysten_US
dc.typeArticleen_US
Appears in Collections:2021



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