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Enantioselective synthesis of α-halo-α-alkylmalonates via phase-transfer catalytic α-alkylation : Enantioselective synthesis of alpha-halo-alpha-alkylmalonates via phase-transfer catalytic alpha-alkylation

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dc.contributor.authorHong, Suckchang-
dc.contributor.authorKim, Minsik-
dc.contributor.authorJung, Myunggi-
dc.contributor.authorHa, Min Woo-
dc.contributor.authorLee, Myungmo-
dc.contributor.authorPark, Yohan-
dc.contributor.authorKim, Mi-hyun-
dc.contributor.authorKim, Taek-Soo-
dc.contributor.authorLee, Jihoon-
dc.contributor.authorPark, Hyeung-geun-
dc.date.accessioned2024-05-14T07:18:19Z-
dc.date.available2024-05-14T07:18:19Z-
dc.date.created2017-11-15-
dc.date.issued2014-03-
dc.identifier.citationOrganic and Biomolecular Chemistry, Vol.12 No.9, pp.1510-1517-
dc.identifier.issn1477-0520-
dc.identifier.urihttps://hdl.handle.net/10371/202023-
dc.description.abstractA new enantioselective synthetic method for alpha-halo-alpha-alkylmalonates is reported. alpha-Alkylation of diphenylmethyl tert-butyl alpha-halomalonates under phase-transfer catalytic conditions (solid KOH, toluene, -40 degrees C) in the presence of (S,S)-3,4,5-trifluorophenyl-NAS bromide (5 mol%) afforded diphenylmethyl tert-butyl alpha-halo-alpha-alkylmalonates in very high chemical yields (up to 99%) and optical yields (up to 93% ee).-
dc.language영어-
dc.publisherRoyal Society of Chemistry-
dc.titleEnantioselective synthesis of α-halo-α-alkylmalonates via phase-transfer catalytic α-alkylation-
dc.title.alternativeEnantioselective synthesis of alpha-halo-alpha-alkylmalonates via phase-transfer catalytic alpha-alkylation-
dc.typeArticle-
dc.identifier.doi10.1039/c3ob42107d-
dc.citation.journaltitleOrganic and Biomolecular Chemistry-
dc.identifier.wosid000330793000017-
dc.identifier.scopusid2-s2.0-84894186519-
dc.citation.endpage1517-
dc.citation.number9-
dc.citation.startpage1510-
dc.citation.volume12-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorHong, Suckchang-
dc.contributor.affiliatedAuthorPark, Hyeung-geun-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusQUATERNARY STEREOGENIC CENTERS-
dc.subject.keywordPlus1,3-DICARBONYL COMPOUNDS-
dc.subject.keywordPlusCONJUGATE ADDITION-
dc.subject.keywordPlusMICHAEL REACTION-
dc.subject.keywordPlusBUILDING-BLOCKS-
dc.subject.keywordPlusAMINO-ACIDS-
dc.subject.keywordPlusESTERS-
dc.subject.keywordPlusCONSTRUCTION-
dc.subject.keywordPlusNITROALKENES-
dc.subject.keywordPlusFLUORINATION-
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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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