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기정민

Kee, Jung-Min
Bioorganic and Chembio Lab.
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DC Field Value Language
dc.citation.endPage 2364 -
dc.citation.number 15 -
dc.citation.startPage 2360 -
dc.citation.title SYNTHESIS-STUTTGART -
dc.contributor.author Lee, Hee-Yoon -
dc.contributor.author Kim, Hyoun Young -
dc.contributor.author Kim, Byung Gyu -
dc.contributor.author Kee, Jung-Min -
dc.date.accessioned 2023-12-22T09:11:59Z -
dc.date.available 2023-12-22T09:11:59Z -
dc.date.created 2015-07-29 -
dc.date.issued 2007-07 -
dc.description.abstract The dimerization reaction of oxidopyrylium ions produces doubly bridged eight-membered carbocyclic rings stereoselectively according to the substitution pattern around the pyrylium ring. © Georg Thieme Verlag Stuttgart. -
dc.identifier.bibliographicCitation SYNTHESIS-STUTTGART, no.15, pp.2360 - 2364 -
dc.identifier.doi 10.1055/s-2007-983770 -
dc.identifier.issn 0039-7881 -
dc.identifier.scopusid 2-s2.0-34547782239 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/13347 -
dc.identifier.url https://www.thieme-connect.de/products/ejournals/html/10.1055/s-2007-983770 -
dc.identifier.wosid 000248806600017 -
dc.language 영어 -
dc.publisher GEORG THIEME VERLAG KG -
dc.title.alternative The stereoselective dimerization reaction of oxidopyrylium ions -
dc.title The stereoselective dimerization reaction of oxidopyrylium ions -
dc.type Article -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor cycloadditions -
dc.subject.keywordAuthor oxidopyrylium ion -
dc.subject.keywordAuthor substituent effects -
dc.subject.keywordAuthor dimerizations -
dc.subject.keywordAuthor stereoselectivity -
dc.subject.keywordPlus RINGS -
dc.subject.keywordPlus CYCLOADDITIONS -
dc.subject.keywordPlus ROUTE -

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