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dc.contributor.author하정미-
dc.date.accessioned2023-08-23T01:17:10Z-
dc.date.available2023-08-23T01:17:10Z-
dc.date.issued2010-09-
dc.identifier.citationTETRAHEDRON LETTERS, v. 51, NO. 35, Page. 4609-4611-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S004040391001049X?via%3Dihuben_US
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/186147-
dc.description.abstractA facile one-step transformation of methylsulfanyl and arylsulfanyl groups on pyrimidine ring system into the corresponding chloride group was achieved using sulfuryl chloride in acetonitrile/dichloromethane. (C) 2010 Elsevier Ltd. All rights reserved.-
dc.languageen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectmethyl group-
dc.subjectdichloromethane-
dc.subjectpolycyclic aromatic hydrocarbon derivative-
dc.subjectsulfur derivative-
dc.subjectliquid chromatography-
dc.subjectquantum yield-
dc.subjectarticle-
dc.subjectbiotransformation-
dc.subjectpyrimidine derivative-
dc.subjectreaction analysis-
dc.subjectmass spectrometry-
dc.subjectreaction time-
dc.subjectacetonitrile-
dc.subjectchlor-
dc.titleThe efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride-
dc.typeArticle-
dc.relation.no35-
dc.relation.volume51-
dc.identifier.doi10.1016/j.tetlet.2010.06.056-
dc.relation.page4609-4611-
dc.relation.journalTETRAHEDRON LETTERS-
dc.contributor.googleauthorHam, Young Jin-
dc.contributor.googleauthorLee, Duck-Hyung-
dc.contributor.googleauthorChoi, Hwan Geun-
dc.contributor.googleauthorHah, Jung-Mi-
dc.contributor.googleauthorSim, Taebo-
dc.sector.campusE-
dc.sector.daehak약학대학-
dc.sector.department약학과-
dc.identifier.pidjhah-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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