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Cited 201 time in webofscience Cited 199 time in scopus
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dc.contributor.authorYoo, EJ-
dc.contributor.authorBae, I-
dc.contributor.authorCho, SH-
dc.contributor.authorHan, H-
dc.contributor.authorChang, S-
dc.date.accessioned2016-03-31T08:03:07Z-
dc.date.available2016-03-31T08:03:07Z-
dc.date.created2014-07-31-
dc.date.issued2006-03-30-
dc.identifier.issn1523-7060-
dc.identifier.other2006-OAK-0000030133-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/14450-
dc.description.abstractIt is shown that N-sulfonylimidates can be efficiently prepared by a three-component coupling of terminal alkynes, sulfonyl azides, and alcohols with use of a copper catalyst and an amine base. The reaction is characterized by mild conditions, high selectivity, and tolerance with various functional groups. Facile transformation of imidates to amidines was also achieved by sodium cyanide. Additionally, a protocol for the extremely efficient Pd-catalyzed [3,3]-sigmatropic rearrangement of allylic sulfonimidates to N-allylic sulfonamides has been developed.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.relation.isPartOfORGANIC LETTERS-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectTERMINAL ALKYNES-
dc.subjectAZIDE-
dc.subjectREARRANGEMENT-
dc.subjectCHEMISTRY-
dc.subjectALCOHOL-
dc.subjectAMINES-
dc.titleA Facile Access to N-Sulfonylimidates and Their Synthetic Utility for the Transformation to Amidines and Amides-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1021/OL060056J-
dc.author.googleYoo, EJ-
dc.author.googleBae, I-
dc.author.googleCho, SH-
dc.author.googleHan, H-
dc.author.googleChang, S-
dc.relation.volume8-
dc.relation.issue7-
dc.relation.startpage1347-
dc.relation.lastpage1350-
dc.contributor.id11362690-
dc.relation.journalORGANIC LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationORGANIC LETTERS, v.8, no.7, pp.1347 - 1350-
dc.identifier.wosid000236397000024-
dc.date.tcdate2019-01-01-
dc.citation.endPage1350-
dc.citation.number7-
dc.citation.startPage1347-
dc.citation.titleORGANIC LETTERS-
dc.citation.volume8-
dc.contributor.affiliatedAuthorCho, SH-
dc.identifier.scopusid2-s2.0-33645942102-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc172-
dc.description.scptc161*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusAZIDE-
dc.subject.keywordPlusALKYNE-
dc.subject.keywordPlusCHEMISTRY-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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