Convergent paired electrolysis for zinc-mediated diastereoselective cinnamylation of a-amino esters

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dc.contributor.authorPark, Hahyounko
dc.contributor.authorKim, Minjunko
dc.contributor.authorKang, Jungtaekko
dc.contributor.authorSong, Hyunjoonko
dc.contributor.authorKim, Hyunwooko
dc.date.accessioned2023-05-13T05:00:25Z-
dc.date.available2023-05-13T05:00:25Z-
dc.date.created2023-05-12-
dc.date.created2023-05-12-
dc.date.created2023-05-12-
dc.date.issued2023-05-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.59, no.36, pp.5447 - 5450-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/306802-
dc.description.abstractA paired electrochemical method is presented for the one-pot synthesis of ?,d-unsaturated a-amino esters. The method involves the in situ generation of organozinc reagents through zinc chloride reduction on the nickel cathode and the TEMPO-mediated oxidation of amino esters on the carbon anode. The presence of an ester moiety in the amine substrate was found to be crucial for achieving high diastereoselectivity.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleConvergent paired electrolysis for zinc-mediated diastereoselective cinnamylation of a-amino esters-
dc.typeArticle-
dc.identifier.wosid000973427700001-
dc.identifier.scopusid2-s2.0-85153110256-
dc.type.rimsART-
dc.citation.volume59-
dc.citation.issue36-
dc.citation.beginningpage5447-
dc.citation.endingpage5450-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/d3cc01197f-
dc.contributor.localauthorSong, Hyunjoon-
dc.contributor.localauthorKim, Hyunwoo-
dc.contributor.nonIdAuthorKim, Minjun-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCARBONYL-COMPOUNDS-
dc.subject.keywordPlusSYNTHETIC APPLICATIONS-
dc.subject.keywordPlusALLYLATION-
dc.subject.keywordPlusCATALYSIS-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusALDEHYDES-
dc.subject.keywordPlusIMINES-
dc.subject.keywordPlusTOOLS-
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