DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, H | - |
dc.contributor.author | Rhee, YH | - |
dc.date.accessioned | 2015-06-25T03:36:40Z | - |
dc.date.available | 2015-06-25T03:36:40Z | - |
dc.date.created | 2013-02-22 | - |
dc.date.issued | 2012-12 | - |
dc.identifier.issn | 0936-5214 | - |
dc.identifier.other | 2015-OAK-0000026526 | en_US |
dc.identifier.uri | https://oasis.postech.ac.kr/handle/2014.oak/12961 | - |
dc.description.abstract | Developing chemical reactions that rapidly introduce molecular diversity in a controlled manner represents a prime goal in synthetic organic chemistry. In this regard, our recent studies on the asymmetric synthesis and utilization of stereodefined N,O-acetal opens up a conceptually new methodology. The synthesis of labile N,O-acetals was accomplished by highly efficient and chemoselective Pd-catalyzed asymmetric hydroamination of alkoxyallenes. Furthermore, the utility of the stereodefined N,O-acetals as a stereodiversity-generating element was established by the gold-catalyzed cycloisomerization. In addition to these results, new aspects of the N,O-acetals as diversity-generating elements are also discussed. | - |
dc.description.statementofresponsibility | open | en_US |
dc.language | English | - |
dc.publisher | GEORG THIEME VERLAG KG | - |
dc.relation.isPartOf | SYNLETT | - |
dc.rights | BY_NC_ND | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.0/kr | en_US |
dc.title | A Perspective on the Stereodefined N,O-Acetals: Synthesis and Potential Applications | - |
dc.type | Article | - |
dc.contributor.college | 화학과 | en_US |
dc.identifier.doi | 10.1055/S-0032-1317478 | - |
dc.author.google | Kim, H | en_US |
dc.author.google | Rhee, YH | en_US |
dc.relation.issue | 20 | en_US |
dc.relation.startpage | 2875 | en_US |
dc.relation.lastpage | 2879 | en_US |
dc.contributor.id | 10153778 | en_US |
dc.relation.journal | SYNLETT | en_US |
dc.relation.index | SCI급, SCOPUS 등재논문 | en_US |
dc.collections.name | Journal Papers | en_US |
dc.type.rims | ART | - |
dc.identifier.bibliographicCitation | SYNLETT, no.20, pp.2875 - 2879 | - |
dc.identifier.wosid | 000312487700002 | - |
dc.date.tcdate | 2019-01-01 | - |
dc.citation.endPage | 2879 | - |
dc.citation.number | 20 | - |
dc.citation.startPage | 2875 | - |
dc.citation.title | SYNLETT | - |
dc.contributor.affiliatedAuthor | Rhee, YH | - |
dc.identifier.scopusid | 2-s2.0-84868244994 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.wostc | 16 | - |
dc.description.scptc | 16 | * |
dc.date.scptcdate | 2018-10-274 | * |
dc.type.docType | Article | - |
dc.subject.keywordPlus | ENANTIOSELECTIVE INTRAMOLECULAR HYDROAMINATION | - |
dc.subject.keywordPlus | ASYMMETRIC ALLYLIC ALKYLATION | - |
dc.subject.keywordPlus | N-ACYLIMINIUM ION | - |
dc.subject.keywordPlus | INTERMOLECULAR HYDROAMINATION | - |
dc.subject.keywordPlus | STEREOCONTROLLED SYNTHESIS | - |
dc.subject.keywordPlus | GOLD | - |
dc.subject.keywordPlus | METATHESIS | - |
dc.subject.keywordPlus | ALCOHOLS | - |
dc.subject.keywordPlus | ALLENES | - |
dc.subject.keywordPlus | PIPERIDINES | - |
dc.subject.keywordAuthor | hydroamination | - |
dc.subject.keywordAuthor | allenes | - |
dc.subject.keywordAuthor | N,O-acetal | - |
dc.subject.keywordAuthor | piperidines | - |
dc.subject.keywordAuthor | diversity | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
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