Spectral correlation of synthesized ethyl-4-(subs. phenyl)-6-methyl-2-oxo (or thio)-1, 2, 3, 4-tetrahydropyrimidine-5-carboxylate

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DC Field	Value	Language
dc.contributor.author	Halim, Md. E.	-
dc.contributor.author	Khan, M. N.	-
dc.contributor.author	Shaha, U.	-
dc.contributor.author	Rahman, M. H.	-
dc.contributor.author	Akhter, K.	-
dc.contributor.author	Ahmed, S. M.	-
dc.date.accessioned	2025-02-26T09:45:53Z	-
dc.date.available	2025-02-26T09:45:53Z	-
dc.date.issued	2024-12-30	-
dc.identifier.citation	25	en_US
dc.identifier.issn	0304-9809	-
dc.identifier.uri	http://dspace.aiub.edu:8080/jspui/handle/123456789/2604	-
dc.description	Ok	en_US
dc.description.abstract	Urea or thiourea, ethyl acetoacetate, and substituted aromatic aldehydes were combined in a one-pot Biginelli coupling reaction to create a few 1, 2, 3, 4-tetrahydro pyrimidine-5-carboxylate derivatives without any unsafe organic solvent. The catalyst used for this reaction was nickel nitrate hexahydrate [Ni(NO3)2.6(H2O)]. The elemental analyses, mass spectral data, 1H-NMR, 13C-NMR, UV, and IR were used to characterize the separated pure products.	en_US
dc.description.sponsorship	N/A	en_US
dc.language.iso	en	en_US
dc.publisher	Bangladesh Council of Scientific and Industrial Research (BCSIR)	en_US
dc.relation.ispartofseries	59;4	-
dc.subject	Biginelli reaction; Solvent free condition; Urea; Thiourea; Substituted aromatic aldehydes	en_US
dc.title	Spectral correlation of synthesized ethyl-4-(subs. phenyl)-6-methyl-2-oxo (or thio)-1, 2, 3, 4-tetrahydropyrimidine-5-carboxylate	en_US
dc.type	Article	en_US
Appears in Collections:	Publication: Journal

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