Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이상기 | * |
dc.date.accessioned | 2016-11-18T02:11:40Z | - |
dc.date.available | 2016-11-18T02:11:40Z | - |
dc.date.issued | 2016 | * |
dc.identifier.issn | 0022-3263 | * |
dc.identifier.other | OAK-19580 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/232705 | - |
dc.description.abstract | A highly efficient method for the one-pot synthesis of stereocontrolled (Z)-3-methyleneisoindolin-1-ones was developed starting from 2-bromoarylnitriles via tandem sequential reaction with a Reformatsky reagent (Blaise reaction), followed by Pd-catalyzed intramolecular aminocarbonylation with carbon monoxide at 1 atm pressure. It has been found that the conformational flexibility of the bisphophine ligand is of great importance to the success of this tandem aminocarbonylation reaction. © 2016 American Chemical Society. | * |
dc.language | English | * |
dc.publisher | American Chemical Society | * |
dc.title | Pd-Catalyzed Aminocarbonylation of the Blaise Reaction Intermediate: One-Pot Synthesis of (Z)-3-Methyleneisoindolin-1-ones from Nitriles | * |
dc.type | Article | * |
dc.relation.issue | 20 | * |
dc.relation.volume | 81 | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 10094 | * |
dc.relation.lastpage | 10098 | * |
dc.relation.journaltitle | Journal of Organic Chemistry | * |
dc.identifier.doi | 10.1021/acs.joc.6b02095 | * |
dc.identifier.wosid | WOS:000386187500064 | * |
dc.identifier.scopusid | 2-s2.0-84992410794 | * |
dc.author.google | Xuan Z. | * |
dc.author.google | Jung D.J. | * |
dc.author.google | Jeon H.J. | * |
dc.author.google | Lee S.-G. | * |
dc.contributor.scopusid | 이상기(15082786300) | * |
dc.date.modifydate | 20240123104103 | * |