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A Flow Microreactor System Enables Organolithium Reactions without Protecting Alkoxycarbonyl Groups

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dc.contributor.author김희진-
dc.date.accessioned2022-04-11T18:42:32Z-
dc.date.available2022-04-11T18:42:32Z-
dc.date.created2022-04-08-
dc.date.issued2010-09-
dc.identifier.issn0947-6539-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/140050-
dc.description.abstractA flow microreactor system consisting of micromixers and microtube reactors provides an effective tool for the generation and reactions of aryllithiums bearing an alkoxycarbonyl group at para-, meta-, and ortho-positions. Alkyl p- and m-lithiobenzoates were generated by the I/Li exchange reaction with PhLi. The Br/Li exchange reactions with sBuLi were unsuccessful. Subsequent reactions of the resulting aryllithiums with electrophiles gave the desired products in good yields. On the other hand, alkyl o-lithiobenzoates were successfully generated by the Br/Li exchange reaction with sBuLi. Subsequent reactions with electrophiles gave the desired products in good yields.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleA Flow Microreactor System Enables Organolithium Reactions without Protecting Alkoxycarbonyl Groups-
dc.typeArticle-
dc.contributor.affiliatedAuthor김희진-
dc.identifier.doi10.1002/chem.201000876-
dc.identifier.bibliographicCitationCHEMISTRY-A EUROPEAN JOURNAL, v.16, no.36, pp.11167 - 11177-
dc.relation.isPartOfCHEMISTRY-A EUROPEAN JOURNAL-
dc.citation.titleCHEMISTRY-A EUROPEAN JOURNAL-
dc.citation.volume16-
dc.citation.number36-
dc.citation.startPage11167-
dc.citation.endPage11177-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordAuthoraryllithium-
dc.subject.keywordAuthorflash chemistry-
dc.subject.keywordAuthormicroreactors-
dc.subject.keywordAuthororganometallic compounds-
dc.subject.keywordAuthorprotecting groups-
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