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Park, Cheol-Min
Synthetic & Medicinal Chemistry Lab
Research Interests
  • Organic synthesis, medicinal chemistry, chemical biology

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BETA-ALKOXYACRYLATES IN RADICAL CYCLIZATIONS - REMARKABLY EFFICIENT OXACYCLE SYNTHESIS

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dc.contributor.author LEE, E ko
dc.contributor.author TAE, JS ko
dc.contributor.author LEE, C ko
dc.contributor.author Park, Cheol-Min ko
dc.date.available 2014-11-11T00:16:46Z -
dc.date.created 2014-11-10 ko
dc.date.issued 1993-07 ko
dc.identifier.citation TETRAHEDRON LETTERS, v.34, no.30, pp.4831 - 4834 ko
dc.identifier.issn 0040-4039 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8577 -
dc.description.abstract Beta-alkoxyacrylates were found to be exceptionally efficient radical acceptors in radical-mediated intramolecular cyclizations. For example, reaction of 5-bromo-2-pentanol with ethyl propiolate, tributylstannane-mediated radical cyclization, and hydrolysis yielded (+/-)-(cis-6-methyltetrahydropyran-2-yl)acetic acid, a known component of civet. ko
dc.description.statementofresponsibility close -
dc.language 영어 ko
dc.publisher PERGAMON-ELSEVIER SCIENCE LTD ko
dc.title BETA-ALKOXYACRYLATES IN RADICAL CYCLIZATIONS - REMARKABLY EFFICIENT OXACYCLE SYNTHESIS ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-0027302923 ko
dc.identifier.wosid A1993LN88200028 ko
dc.type.rims ART ko
dc.description.wostc 83 *
dc.description.scopustc 74 *
dc.date.tcdate 2015-05-06 *
dc.date.scptcdate 2014-11-10 *
dc.identifier.doi 10.1016/S0040-4039(00)74101-3 ko
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0027302923 ko
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