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Cited 6 time in webofscience Cited 6 time in scopus
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dc.contributor.authorHan, J-
dc.contributor.authorRhee, YH-
dc.contributor.authorPark, J-
dc.date.accessioned2016-03-31T07:41:05Z-
dc.date.available2016-03-31T07:41:05Z-
dc.date.created2015-01-22-
dc.date.issued2014-12-20-
dc.identifier.issn0253-2964-
dc.identifier.other2015-OAK-0000031541-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/13900-
dc.description.abstractA new method for the synthesis of 2,2-dimethyl-6-substituted 4-piperidone was developed; two equivalents of acetone were annulated with N-unsubstituted imines in-situ generated from benzyl azides using a ruthenium catalyst in the presence of L-proline.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisher대한화학회-
dc.relation.isPartOfBulletin of the Korean Chemical Society-
dc.titleSynthesis of Piperidones from Benzyl Azides and Acetone-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1002/BKCS.10180-
dc.author.googleHan, J-
dc.author.googleRhee, YH-
dc.author.googlePark, J-
dc.relation.volume35-
dc.relation.issue12-
dc.relation.startpage3433-
dc.relation.lastpage3436-
dc.contributor.id10153778-
dc.relation.journalBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBulletin of the Korean Chemical Society, v.35, no.12, pp.3433 - 3436-
dc.identifier.wosid000346113000006-
dc.date.tcdate2019-01-01-
dc.citation.endPage3436-
dc.citation.number12-
dc.citation.startPage3433-
dc.citation.titleBulletin of the Korean Chemical Society-
dc.citation.volume35-
dc.contributor.affiliatedAuthorRhee, YH-
dc.contributor.affiliatedAuthorPark, J-
dc.identifier.scopusid2-s2.0-84920096695-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc3-
dc.description.isOpenAccessY-
dc.type.docTypeArticle-
dc.subject.keywordPlusCATALYZED ASYMMETRIC 1,4-ADDITION-
dc.subject.keywordPlusCONJUGATE ADDITION-REACTIONS-
dc.subject.keywordPlusN-UNSUBSTITUTED IMINES-
dc.subject.keywordPlusONE-POT SYNTHESIS-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusSTEREOSELECTIVE-SYNTHESIS-
dc.subject.keywordPlusMICHAEL REACTIONS-
dc.subject.keywordPlusROOM-TEMPERATURE-
dc.subject.keywordPlusALKYL AZIDES-
dc.subject.keywordPlusREAGENTS-
dc.subject.keywordAuthor4-Piperidone-
dc.subject.keywordAuthorN-Unsubstituted imine-
dc.subject.keywordAuthorBenzyl azide-
dc.subject.keywordAuthorSynthetic method-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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