Chemoselective O-Benzylation of the Propargylic Hydroxy Group in Polyols
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, Ji Ho | - |
dc.contributor.author | Oh, Chang Ho | - |
dc.date.accessioned | 2022-07-07T13:41:14Z | - |
dc.date.available | 2022-07-07T13:41:14Z | - |
dc.date.created | 2021-05-12 | - |
dc.date.issued | 2012-10 | - |
dc.identifier.issn | 1434-193X | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/144705 | - |
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. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.title | Chemoselective O-Benzylation of the Propargylic Hydroxy Group in Polyols | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Oh, Chang Ho | - |
dc.identifier.doi | 10.1002/ejoc.201201086 | - |
dc.identifier.scopusid | 2-s2.0-84867607642 | - |
dc.identifier.wosid | 000309923400005 | - |
dc.identifier.bibliographicCitation | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, v.2012, no.30, pp.5913 - 5917 | - |
dc.relation.isPartOf | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | - |
dc.citation.title | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | - |
dc.citation.volume | 2012 | - |
dc.citation.number | 30 | - |
dc.citation.startPage | 5913 | - |
dc.citation.endPage | 5917 | - |
dc.type.rims | ART | - |
dc.type.docType | Review | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | HIGHLY EFFICIENT CATALYST | - |
dc.subject.keywordPlus | STEREOSELECTIVE-SYNTHESIS | - |
dc.subject.keywordPlus | LITHIUM PERCHLORATE | - |
dc.subject.keywordPlus | ENANTIOSELECTIVE SYNTHESIS | - |
dc.subject.keywordPlus | SELECTIVE PROTECTION | - |
dc.subject.keywordPlus | TRIALKYLSILYL ETHER | - |
dc.subject.keywordPlus | RECYCLABLE CATALYST | - |
dc.subject.keywordPlus | ALCOHOLS | - |
dc.subject.keywordPlus | ACYLATION | - |
dc.subject.keywordPlus | DEPROTECTION | - |
dc.subject.keywordAuthor | Chemoselectivity | - |
dc.subject.keywordAuthor | Protecting groups | - |
dc.subject.keywordAuthor | Alkynes | - |
dc.subject.keywordAuthor | Alcohols | - |
dc.subject.keywordAuthor | Benzyl ether | - |
dc.identifier.url | https://chemistry-europe.onlinelibrary.wiley.com/doi/epdf/10.1002/ejoc.201201086 | - |
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