Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이상기 | * |
dc.contributor.author | 김주현 | * |
dc.date.accessioned | 2016-08-27T04:08:56Z | - |
dc.date.available | 2016-08-27T04:08:56Z | - |
dc.date.issued | 2015 | * |
dc.identifier.issn | 0022-3263 | * |
dc.identifier.other | OAK-15442 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/217487 | - |
dc.description.abstract | A novel Pd-catalyzed Ullmann-type homocoupling reaction of the Blaise reaction intermediate generated by the reaction of 2-bromo arylnitriles and a Reformatsky reagent has been developed for one-pot synthesis of enamino esterfunctionalized biaryls 2 in good yields. The 2,2'-substituted enamine moieties of the coupling products could be cyclized under acidic conditions through the conjugate addition/deamination cascade to afford the seven-membered N-heterocyclics 3 with biaryl backbone in excellent yields. | * |
dc.language | English | * |
dc.publisher | AMER CHEMICAL SOC | * |
dc.title | Tandem Blaise/Palladium-Catalyzed Ullmann Coupling for the One-Pot Synthesis of Enamino Ester-Functionalized Biaryls from Nitriles | * |
dc.type | Article | * |
dc.relation.issue | 15 | * |
dc.relation.volume | 80 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 7824 | * |
dc.relation.lastpage | 7829 | * |
dc.relation.journaltitle | JOURNAL OF ORGANIC CHEMISTRY | * |
dc.identifier.doi | 10.1021/acs.joc.5b01375 | * |
dc.identifier.wosid | WOS:000359393500058 | * |
dc.identifier.scopusid | 2-s2.0-84938769410 | * |
dc.author.google | Xuan, Zi | * |
dc.author.google | Kim, Ju Hyun | * |
dc.author.google | Lee, Sang-gi | * |
dc.contributor.scopusid | 이상기(15082786300) | * |
dc.contributor.scopusid | 김주현(57207894284) | * |
dc.date.modifydate | 20240123104103 | * |