Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 오창호 | - |
dc.date.accessioned | 2018-04-16T03:28:10Z | - |
dc.date.available | 2018-04-16T03:28:10Z | - |
dc.date.issued | 2012-10 | - |
dc.identifier.citation | European journal of organic chemistry, 2012, 2012(30), pp.5913 - 5917 | en_US |
dc.identifier.issn | 1434-193X | - |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201201086 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.11754/67669 | - |
dc.description.abstract | We 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.iso | en | en_US |
dc.publisher | John Wiley & Sons, Ltd | en_US |
dc.subject | Chemoselectivity | en_US |
dc.subject | Protecting groups | en_US |
dc.subject | Alkynes | en_US |
dc.subject | Alcohols | en_US |
dc.subject | Benzyl ether | en_US |
dc.title | Chemoselective O-Benzylation of the Propargylic Hydroxy Group in Polyols | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1002/ejoc.201201086 | - |
dc.relation.page | 5913-5917 | - |
dc.relation.journal | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | - |
dc.contributor.googleauthor | Lee, J. H. | - |
dc.contributor.googleauthor | Oh, C. H. | - |
dc.relation.code | 2012203042 | - |
dc.sector.campus | S | - |
dc.sector.daehak | COLLEGE OF NATURAL SCIENCES[S] | - |
dc.sector.department | DEPARTMENT OF CHEMISTRY | - |
dc.identifier.pid | changho | - |
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