Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 류재상 | * |
dc.date.accessioned | 2016-08-28T12:08:19Z | - |
dc.date.available | 2016-08-28T12:08:19Z | - |
dc.date.issued | 2010 | * |
dc.identifier.issn | 0022-3263 | * |
dc.identifier.other | OAK-6618 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/220826 | - |
dc.description.abstract | Novel 1,3-dialkyl-1,2,3-triazolium ionic liquids were synthesized via click reactions using 1-trimethylsilylacetylene and alkyl azides and were efficient reaction media for the Baylis-Hillman reaction. The problems associated with deprotonation of the C-2 hydrogen of [bmim][PF6] could be suppressed in the reaction of [bmTr][PF6] or [bmTr][NTf2]. 1,3-Dialkyl-1,2,3-triazolium ionic liquids are chemically inert under basic conditions and more suitable media for the reactions involving bases than the common 1,3-dialkylimidazolium ionic liquids. © 2010 American Chemical Society. | * |
dc.language | English | * |
dc.title | Synthesis of 1,3-Dialkyl-1,2,3-triazolium ionic liquids and their applications to the baylis-hillman reaction | * |
dc.type | Article | * |
dc.relation.issue | 12 | * |
dc.relation.volume | 75 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 4183 | * |
dc.relation.lastpage | 4191 | * |
dc.relation.journaltitle | Journal of Organic Chemistry | * |
dc.identifier.doi | 10.1021/jo100618d | * |
dc.identifier.wosid | WOS:000278560700026 | * |
dc.identifier.scopusid | 2-s2.0-77953507131 | * |
dc.author.google | Jeong Y. | * |
dc.author.google | Ryu J.-S. | * |
dc.contributor.scopusid | 류재상(36081118200) | * |
dc.date.modifydate | 20231120165709 | * |