Zn2+/MCM-41 catalyzed Biginelli reaction of heteroaryl aldehydes and evaluation of the antimicrobial activity and cytotoxicity of the pyrimidone products
dc.contributor.author | Ghasemi, Z | |
dc.contributor.author | Orafa, FF | |
dc.contributor.author | Pirouzmand, M | |
dc.contributor.author | Zarrini, G | |
dc.contributor.author | Kojanag, BN | |
dc.contributor.author | Salehi, R | |
dc.date.accessioned | 2018-08-26T07:41:35Z | |
dc.date.available | 2018-08-26T07:41:35Z | |
dc.date.issued | 2015 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/47587 | |
dc.description.abstract | The three component Biginelli condensation of various aryl aldehydes, 1,3-dicarbonyls and urea was investigated in the presence of free or MCM-41 supported ZnNO3. The pyrimidone products, which were obtained under solvent-free conditions, were evaluated for antibacterial and antifungal activities as well as their cytotoxicities. (C) 2015 Elsevier Ltd. All rights reserved. | |
dc.language.iso | English | |
dc.relation.ispartof | TETRAHEDRON LETTERS | |
dc.subject | Biginelli reaction | |
dc.subject | Solvent-free conditions | |
dc.subject | MCM-41 | |
dc.subject | 3,4-Dihydropyrimidones | |
dc.title | Zn2+/MCM-41 catalyzed Biginelli reaction of heteroaryl aldehydes and evaluation of the antimicrobial activity and cytotoxicity of the pyrimidone products | |
dc.type | Article | |
dc.citation.volume | 56 | |
dc.citation.issue | 46 | |
dc.citation.spage | 6393 | |
dc.citation.epage | 6396 | |
dc.citation.index | Web of science | |
dc.identifier.DOI | https://doi.org/10.1016/j.tetlet.2015.09.143 |
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