Please use this identifier to cite or link to this item: http://10.9.150.37:8080/dspace//handle/atmiyauni/1640
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dc.contributor.authorLalpara, J. N.-
dc.contributor.authorHadiyal, S. D.-
dc.contributor.authorRadia, A. J.-
dc.contributor.authorDhalani, J. M.-
dc.contributor.authorDubal, G. G.-
dc.date.accessioned2024-11-18T09:57:07Z-
dc.date.available2024-11-18T09:57:07Z-
dc.date.issued2020-12-01-
dc.identifier.citationLalpara, J. N., Hadiyal, S. D., Radia, A. J., Dhalani, J. M., & Dubal, G. G. (2022). Design and rapid microwave irradiated one-pot synthesis of tetrahydropyrimidine derivatives and their screening in vitro antidiabetic activity. Polycyclic Aromatic Compounds, 42(6), 3063-3078.en_US
dc.identifier.urihttp://10.9.150.37:8080/dspace//handle/atmiyauni/1640-
dc.description.abstractA rapid and efficient method has been developed for one-pot synthesis of some newly designed tetrahydropyrimidine derivatives with aid of 1,3,4-oxadiazole containing aldehyde, substituted acetoacetanilide and thiourea/guanidine in the occurrence of microwave irradiation. The significant yield of products, atom economy, less time consuming, and catalyst-free synthesis were considered preferences of microwave irradiation. All synthesized compounds were characterized by 1H NMR, 13C NMR, IR, and mass spectrometry techniques. All synthesized compounds were evaluated bioassay for in vitro antidiabetic screening viz α-amylase inhibition strategy and checked their potency against standard reference drug acarbose.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francis Group, LLC / Polycyclic Aromatic Compoundsen_US
dc.relation.ispartofseries;42(6), 3063-3078-
dc.subjectBiginellien_US
dc.subjectpolycyclic aldehydeen_US
dc.subjecttetrahydropyrimidineen_US
dc.subjectantidiabeticen_US
dc.titleDesign and rapid microwave irradiated one-pot synthesis of tetrahydropyrimidine derivatives and their screening in vitro antidiabetic activityen_US
dc.typeArticleen_US
Appears in Collections:01. Journal Articles

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