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dc.citation.endPage 1735 -
dc.citation.number 9 -
dc.citation.startPage 1733 -
dc.citation.title ANGEWANDTE CHEMIE-INTERNATIONAL EDITION -
dc.citation.volume 47 -
dc.contributor.author Kwon, Min Sang -
dc.contributor.author Woo, Sang Kook -
dc.contributor.author Na, Seong Wook -
dc.contributor.author Lee, Eun -
dc.date.accessioned 2023-12-22T09:06:40Z -
dc.date.available 2023-12-22T09:06:40Z -
dc.date.created 2016-06-20 -
dc.date.issued 2008 -
dc.description.abstract The unique 16-membered macrolide (+)-exiguolide (1) was the target of a total synthesis featuring radical and Prins cyclizations of β-alkoxyacrylates, along with ring-closing olefin metathesis. The structure incorporates two cis-2,6-disubstituted oxane rings where one of the rings has an exocyclic enoate group. The successful synthesis of 1, isolated from a marine sponge, led to the unambiguous determination of its absolute stereochemistry. -
dc.identifier.bibliographicCitation ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.47, no.9, pp.1733 - 1735 -
dc.identifier.doi 10.1002/anie.200705018 -
dc.identifier.issn 1433-7851 -
dc.identifier.scopusid 2-s2.0-41049112894 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/19908 -
dc.identifier.url http://onlinelibrary.wiley.com/doi/10.1002/anie.200705018/abstract -
dc.identifier.wosid 000253434300030 -
dc.language 영어 -
dc.publisher WILEY-V C H VERLAG GMBH -
dc.title Total synthesis of (+)-exiguolide -
dc.type Article -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor macrolides -
dc.subject.keywordAuthor natural products -
dc.subject.keywordAuthor total synthesis -
dc.subject.keywordPlus WADSWORTH-EMMONS REACTION -
dc.subject.keywordPlus CHIRAL SYNTHESIS -
dc.subject.keywordPlus CYCLIZATION -
dc.subject.keywordPlus ORGANOBORANES -
dc.subject.keywordPlus EFFICIENT -
dc.subject.keywordPlus ALCOHOLS -
dc.subject.keywordPlus ZN -

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