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dc.citation.endPage 9801 -
dc.citation.number 39 -
dc.citation.startPage 9784 -
dc.citation.title TETRAHEDRON -
dc.citation.volume 63 -
dc.contributor.author Kim, Woo Han -
dc.contributor.author Hong, Sung Kil -
dc.contributor.author Lim, Sang Min -
dc.contributor.author Ju, Min-Ae -
dc.contributor.author Jung, Soon Kyu -
dc.contributor.author Kim, Yong Wook -
dc.contributor.author Jung, Jae Hoon -
dc.contributor.author Kwon, Min Sang -
dc.contributor.author Lee, Eun -
dc.date.accessioned 2023-12-22T09:10:04Z -
dc.date.available 2023-12-22T09:10:04Z -
dc.date.created 2016-06-20 -
dc.date.issued 2007-09 -
dc.description.abstract Total synthesis of IKD-8344 was accomplished via stepwise cyclodimerization of the monomeric seco acid under Yamaguchi conditions. In the synthesis of the monomeric seco acid, Wittig olefination reaction was employed for an efficient bond formation at C7-C8. The threo-trans oxolane unit for the rings a and c was prepared via intramolecular Williamson ether synthesis of the hydroxyl mesylate prepared via asymmetric aldol reaction. Radical cyclization of a beta-alkoxymethacrylate intermediate furnished the threo-cis oxolane unit for the b ring fragment. (C) 2007 Elsevier Ltd. All rights reserved -
dc.identifier.bibliographicCitation TETRAHEDRON, v.63, no.39, pp.9784 - 9801 -
dc.identifier.doi 10.1016/j.tet.2007.07.005 -
dc.identifier.issn 0040-4020 -
dc.identifier.scopusid 2-s2.0-34547821399 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/19896 -
dc.identifier.url http://www.sciencedirect.com/science/article/pii/S0040402007012045 -
dc.identifier.wosid 000252092000026 -
dc.language 영어 -
dc.publisher PERGAMON-ELSEVIER SCIENCE LTD -
dc.title Stereoselective synthesis of (+)-IKD-8344 -
dc.type Article -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus MACRODIOLIDE ANTIBIOTIC IKD-8344 -
dc.subject.keywordPlus RING-CLOSING METATHESIS -
dc.subject.keywordPlus TETRAHYDROFURANS -
dc.subject.keywordPlus ETHERS -

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