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박철민

Park, Cheol-Min
Synthetic and Medicinal Chemistry Lab.
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dc.citation.endPage 7336 -
dc.citation.number 32 -
dc.citation.startPage 7333 -
dc.citation.title ANGEWANDTE CHEMIE-INTERNATIONAL EDITION -
dc.citation.volume 50 -
dc.contributor.author Liu, Yu -
dc.contributor.author Li, Dan -
dc.contributor.author Park, Cheol-Min -
dc.date.accessioned 2023-12-22T06:38:00Z -
dc.date.available 2023-12-22T06:38:00Z -
dc.date.created 2014-11-10 -
dc.date.issued 2011 -
dc.description.abstract Functionalization of enamides under Heck conditions has been limited to those with unsubstituted vinyl groups. By tuning reaction parameters that allow for the balance between stability and reactivity of reactants, the oxidative Heck cross-coupling to produce highly substituted enamides in good to excellent yields was achieved (see scheme). -
dc.identifier.bibliographicCitation ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.50, no.32, pp.7333 - 7336 -
dc.identifier.doi 10.1002/anie.201101550 -
dc.identifier.issn 1433-7851 -
dc.identifier.scopusid 2-s2.0-79960897911 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8539 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79960897911 -
dc.identifier.wosid 000293840400023 -
dc.language 영어 -
dc.publisher WILEY-V C H VERLAG GMBH -
dc.title Stereoselective Synthesis of Highly Substituted Enamides by an Oxidative Heck Reaction -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

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