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Enantioselective synthesis of chiral α-thio-quaternary stereogenic centers via phase-transfer-catalyzed α-alkylation of α-acylthiomalonates : Enantioselective synthesis of chiral alpha-thio-quaternary stereogenic centers via phase-transfer-catalyzed alpha-alkylation of alpha-acylthiomalonates

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dc.contributor.authorHa, Min Woo-
dc.contributor.authorLee, Jun Young-
dc.contributor.authorKim, Do Young-
dc.contributor.authorLee, Geumwoo-
dc.contributor.authorLee, Jae Kyun-
dc.contributor.authorHong, Suckchang-
dc.contributor.authorPark, Hyeung-geun-
dc.date.accessioned2024-05-14T07:17:34Z-
dc.date.available2024-05-14T07:17:34Z-
dc.date.created2018-12-14-
dc.date.issued2018-01-
dc.identifier.citationJournal of Organic Chemistry, Vol.83 No.2, pp.1011-1018-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://hdl.handle.net/10371/202012-
dc.description.abstractAn efficient synthetic method for establishing chiral α-thio-α-quaternary stereogenic center was successfully developed. The enantioselective α-alkylation of α-acylthiomalonates under phase-transfer catalytic conditions [50% aq. KOH, toluene, −20 °C, and (S,S)-3,4,5-trifluorophenyl-NAS bromide] provided the corresponding α-acylthio-α-alkylmalonates in high chemical yields (up to 99%) and high optical yields (up to 98% ee).-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleEnantioselective synthesis of chiral α-thio-quaternary stereogenic centers via phase-transfer-catalyzed α-alkylation of α-acylthiomalonates-
dc.title.alternativeEnantioselective synthesis of chiral alpha-thio-quaternary stereogenic centers via phase-transfer-catalyzed alpha-alkylation of alpha-acylthiomalonates-
dc.typeArticle-
dc.identifier.doi10.1021/acs.joc.7b02605-
dc.citation.journaltitleJournal of Organic Chemistry-
dc.identifier.wosid000423252300045-
dc.identifier.scopusid2-s2.0-85040807884-
dc.citation.endpage1018-
dc.citation.number2-
dc.citation.startpage1011-
dc.citation.volume83-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorHong, Suckchang-
dc.contributor.affiliatedAuthorPark, Hyeung-geun-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusPRACTICAL ASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlusAMINO-
dc.subject.keywordPlusSULFENYLATION-
dc.subject.keywordPlusCONSTRUCTION-
dc.subject.keywordPlusARYLATION-
dc.subject.keywordPlusACIDS-
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Development of methodologies using metal catalyst, Total synthesis of natural products

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