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Cited 2 time in webofscience Cited 3 time in scopus
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A Green Chemical Approach for Iodination of Pyrimidine Derivatives by Mechanical Grinding under Solvent-Free Conditions

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dc.contributor.authorBalasubramaniyam, Thananjeyan-
dc.contributor.authorKim, Byeong-Seon-
dc.contributor.authorPallavi, Badvel-
dc.contributor.authorJin, Ho-Seong-
dc.contributor.authorKim, Sung Kuk-
dc.contributor.authorLee, Joon-Hwa-
dc.date.accessioned2023-01-03T06:00:04Z-
dc.date.available2023-01-03T06:00:04Z-
dc.date.issued2022-10-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/29861-
dc.description.abstractThe iodination of pyrimidines is usually carried out by using toxic reagents under acidic conditions, such as with sulfuric acid and nitric acid. To avoid toxic reagents, we developed a simple and eco-friendly approach for the iodination of pyrimidine derivatives under solvent-free conditions using solid iodine and AgNO3 as an electrophilic iodinating reagent. The advantages of this method are the relatively short reaction time (20-30 min), simple set-up procedure, high yields (70-98%), and environmentally friendly reaction conditions. Our novel approach for the iodination of pyrimidines, as well as a variety of their derivatives, will contribute to the development of nucleobase-related drug candidates.-
dc.language영어-
dc.language.isoENG-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleA Green Chemical Approach for Iodination of Pyrimidine Derivatives by Mechanical Grinding under Solvent-Free Conditions-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/molecules27196386-
dc.identifier.scopusid2-s2.0-85139794148-
dc.identifier.wosid000867986100001-
dc.identifier.bibliographicCitationMolecules, v.27, no.19-
dc.citation.titleMolecules-
dc.citation.volume27-
dc.citation.number19-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusN-IODOSUCCINIMIDE-
dc.subject.keywordPlusNUCLEOSIDES-
dc.subject.keywordPlusIODINE-
dc.subject.keywordPlusARENES-
dc.subject.keywordPlusARYLATION-
dc.subject.keywordPlusNITRATE-
dc.subject.keywordPlusMILD-
dc.subject.keywordAuthorgreen synthesis-
dc.subject.keywordAuthormechanochemistry-
dc.subject.keywordAuthornitrate salts-
dc.subject.keywordAuthorpyrimidine derivatives-
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