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dc.contributor.author오창호-
dc.date.accessioned2018-04-16T03:28:10Z-
dc.date.available2018-04-16T03:28:10Z-
dc.date.issued2012-10-
dc.identifier.citationEuropean journal of organic chemistry, 2012, 2012(30), pp.5913 - 5917en_US
dc.identifier.issn1434-193X-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201201086-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/67669-
dc.description.abstractWe have discovered the highly chemoselective benzylation of propargylic hydroxy groups in the presence of other hydroxy groups under very usual conditions involving benzyl bromide and sodium hydroxide in DMF at room temperature.This methodology has a high synthetic utility for the selective protection of hydroxy groups at the propargylic position among various other hydroxy groups in complex molecules.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons, Ltden_US
dc.subjectChemoselectivityen_US
dc.subjectProtecting groupsen_US
dc.subjectAlkynesen_US
dc.subjectAlcoholsen_US
dc.subjectBenzyl etheren_US
dc.titleChemoselective O-Benzylation of the Propargylic Hydroxy Group in Polyolsen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ejoc.201201086-
dc.relation.page5913-5917-
dc.relation.journalEUROPEAN JOURNAL OF ORGANIC CHEMISTRY-
dc.contributor.googleauthorLee, J. H.-
dc.contributor.googleauthorOh, C. H.-
dc.relation.code2012203042-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidchangho-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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