Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9004
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dc.contributor.authorGuin, Soumitraen_US
dc.contributor.authorMajee, Debashisen_US
dc.contributor.authorBiswas, Soumenen_US
dc.contributor.authorSamanta, Sampaken_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:30:37Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:30:37Z-
dc.date.issued2018-
dc.identifier.citationGuin, S., Majee, D., Biswas, S., & Samanta, S. (2018). Microwave-assisted and base-promoted domino reaction of cyclic N-sulfonyl ketimines with α,β-disubstituted nitroalkenes: A green access to 2-hydroxyarylpyridines. Asian Journal of Organic Chemistry, 7(9), 1810-1814. doi:10.1002/ajoc.201800298en_US
dc.identifier.issn2193-5807-
dc.identifier.otherEID(2-s2.0-85053029350)-
dc.identifier.urihttps://doi.org/10.1002/ajoc.201800298-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9004-
dc.description.abstractMicrowave-assisted and organobase-promoted eco-friendly one-pot protocol has been developed to construct an interesting class of pyridyl-substituted phenols/α-naphthols containing a carboxylate or aroyl group at C2 position on the pyridine ring. A series of N-sulfonyl ketimines and different kinds of bielectrophiles, such as MBH acetates of nitroalkenes/α-arylacetylenyl-β-arylnitroolefins, were involved in this cyclization process, which delivers good to high yields of aforementioned heterocycles and excels with several compatible functionalities. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.sourceAsian Journal of Organic Chemistryen_US
dc.titleMicrowave-Assisted and Base-Promoted Domino Reaction of Cyclic N-Sulfonyl Ketimines with α,β-Disubstituted Nitroalkenes: A Green Access to 2-Hydroxyarylpyridinesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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