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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9209
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dc.contributor.authorMajee, Debashisen_US
dc.contributor.authorBiswas, Soumenen_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.contributor.authorSamanta, Sampaken_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:31:38Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:31:38Z-
dc.date.issued2016-
dc.identifier.citationMajee, D., Biswas, S., Mobin, S. M., & Samanta, S. (2016). Access to 4,6-diarylpicolinates via a domino reaction of cyclic sulfamidate imines with morita-baylis-hillman acetates of Nitroolefins/Nitrodienes. Journal of Organic Chemistry, 81(10), 4378-4385. doi:10.1021/acs.joc.6b00472en_US
dc.identifier.issn0022-3263-
dc.identifier.otherEID(2-s2.0-84971296245)-
dc.identifier.urihttps://doi.org/10.1021/acs.joc.6b00472-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9209-
dc.description.abstractAn interesting domino reaction of 5-membered cyclic sulfamidate imines with a variety of Morita-Baylis-Hillman acetates of nitroolefins/nitrodienes in the presence of DABCO as an organic base at 55 °C is reported for the first time. This new synthetic strategy provides a series of pharmacologically interesting 4,6-diarylpicolinates in high to excellent yields and allows several compatible functionalities on aryl rings. Moreover, the biologically interesting imidazo[1,2-a]pyridine (alpidem derivative) has been prepared in high chemical yield through a unique procedure. © 2016 American Chemical Society.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.sourceJournal of Organic Chemistryen_US
dc.subjectRate constantsen_US
dc.subjectReaction kineticsen_US
dc.subjectAryl ringsen_US
dc.subjectChemical yieldsen_US
dc.subjectDomino reactionsen_US
dc.subjectImidazo[1 ,2-a]pyridineen_US
dc.subjectMorita-baylis-hillmanen_US
dc.subjectNitroolefinsen_US
dc.subjectOrganic baseen_US
dc.subjectSynthetic strategiesen_US
dc.subjectNitrogen compoundsen_US
dc.subject1,4 diazabicyclo[2.2.2]octaneen_US
dc.subject4,6 diarylpicolinate derivativeen_US
dc.subjectacetic acid derivativeen_US
dc.subjectaldehydeen_US
dc.subjectalkadieneen_US
dc.subjectalkeneen_US
dc.subjectimidazo[1,2 a]pyridine derivativeen_US
dc.subjectimineen_US
dc.subjectnitrodiene derivativeen_US
dc.subjectnitroolefin derivativeen_US
dc.subjectnucleophileen_US
dc.subjectorganic compounden_US
dc.subjectpyridine derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectArticleen_US
dc.subjectbiological activityen_US
dc.subjectchemical analysisen_US
dc.subjectchemical modificationen_US
dc.subjectchemical reactionen_US
dc.subjectchemical structureen_US
dc.subjectdomino reactionen_US
dc.subjectone pot synthesisen_US
dc.subjectphysical chemistryen_US
dc.subjectsynthetic biologyen_US
dc.titleAccess to 4,6-Diarylpicolinates via a Domino Reaction of Cyclic Sulfamidate Imines with Morita-Baylis-Hillman Acetates of Nitroolefins/Nitrodienesen_US
dc.typeJournal Articleen_US
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