Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김영미 | * |
dc.contributor.author | 이상기 | * |
dc.date.accessioned | 2016-08-28T12:08:11Z | - |
dc.date.available | 2016-08-28T12:08:11Z | - |
dc.date.issued | 2009 | * |
dc.identifier.issn | 1477-0520 | * |
dc.identifier.other | OAK-5447 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/220147 | - |
dc.description.abstract | An effective and general route for the regioselective synthesis of 1-phenylpyrazoles has been developed from β-enaminoketoesters prepared by tandem Blaise-acylation. This method is applicable to a very broad range of substrates, generating a diverse set of 3-aryl-5-alkyl, 3-alkyl-5-aryl, 3,5-diaryl, and 3,5-dialkyl substituted pyrazoles regioselectively. The dichotomous regioselective synthesis of isotopically discriminated 3-CD 3-5-CH 3 and 3-CH 3-5-CD 3 substituted pyrazoles showcases the power of this protocol. © The Royal Society of Chemistry 2009. | * |
dc.language | English | * |
dc.title | An effective and general method for the highly regioselective synthesis of 1-phenylpyrazoles from β-enaminoketoesters, tandem Blaise-acylation adducts | * |
dc.type | Article | * |
dc.relation.issue | 6 | * |
dc.relation.volume | 7 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 1132 | * |
dc.relation.lastpage | 1136 | * |
dc.relation.journaltitle | Organic and Biomolecular Chemistry | * |
dc.identifier.doi | 10.1039/b820324e | * |
dc.identifier.wosid | WOS:000263922700014 | * |
dc.identifier.scopusid | 2-s2.0-62249157813 | * |
dc.author.google | Ko Y.O. | * |
dc.author.google | Chun Y.S. | * |
dc.author.google | Park C.-L. | * |
dc.author.google | Kim Y. | * |
dc.author.google | Shin H. | * |
dc.author.google | Ahn S. | * |
dc.author.google | Hong J. | * |
dc.author.google | Lee S.-G. | * |
dc.contributor.scopusid | 김영미(57207443602) | * |
dc.contributor.scopusid | 이상기(15082786300) | * |
dc.date.modifydate | 20240301081003 | * |