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Microwave-assisted amination of 3-bromo-2-chloropyridine with various substituted aminoethanols

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dc.contributor.authorKim, Jeong Geun-
dc.contributor.authorYang, Eun Hae-
dc.contributor.authorYoun, Woo Sup-
dc.contributor.authorChoi, Ji Won-
dc.contributor.authorHa, Deok-Chan-
dc.contributor.authorHa, Jae Du-
dc.date.accessioned2021-09-08T01:28:23Z-
dc.date.available2021-09-08T01:28:23Z-
dc.date.created2021-06-14-
dc.date.issued2010-07-28-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/116040-
dc.description.abstractA simple method for microwave-assisted amination of 3-bromo-2-chloropyridine with various substituted aminoethanols is described. The reaction was carried out under microwave irradiation conditions (at 180 degrees C for 1-2 h) and the result was superior in terms of conversion and yield when compared to that of the corresponding conventional heating conditions. (C) 2010 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectARYL CHLORIDES-
dc.subjectBOND FORMATION-
dc.subjectEFFICIENT-
dc.subjectDESIGN-
dc.subjectANTAGONISTS-
dc.subjectINHIBITORS-
dc.subjectCATALYSTS-
dc.subjectLIGANDS-
dc.subjectPOTENT-
dc.titleMicrowave-assisted amination of 3-bromo-2-chloropyridine with various substituted aminoethanols-
dc.typeArticle-
dc.contributor.affiliatedAuthorHa, Deok-Chan-
dc.identifier.doi10.1016/j.tetlet.2010.05.021-
dc.identifier.scopusid2-s2.0-77953683768-
dc.identifier.wosid000279817400005-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.51, no.30, pp.3886 - 3889-
dc.relation.isPartOfTETRAHEDRON LETTERS-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume51-
dc.citation.number30-
dc.citation.startPage3886-
dc.citation.endPage3889-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusARYL CHLORIDES-
dc.subject.keywordPlusBOND FORMATION-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusANTAGONISTS-
dc.subject.keywordPlusINHIBITORS-
dc.subject.keywordPlusCATALYSTS-
dc.subject.keywordPlusLIGANDS-
dc.subject.keywordPlusPOTENT-
dc.subject.keywordAuthorMicrowave-assisted amination-
dc.subject.keywordAuthor3-Bromo-2-chloropyridine-
dc.subject.keywordAuthorAminoethanol-
dc.subject.keywordAuthorPyrido[1,4]oxazine-
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