Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 윤주영 | * |
dc.date.accessioned | 2016-12-13T02:12:29Z | - |
dc.date.available | 2016-12-13T02:12:29Z | - |
dc.date.issued | 2008 | * |
dc.identifier.issn | 0040-4039 | * |
dc.identifier.other | OAK-4877 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/233122 | - |
dc.description.abstract | 5-Substituted dipyrromethane analogues (8), (23) and (25) were synthesized by the reaction of 2-vinylpyrroles, 2-vinylthiophene or 2-vinylbenzenes with excess pyrrole in the presence of Lewis acids. Accordingly, tripyrromethane analogues could be obtained by starting with 2,5-divinyl thiophene or 2,6-divinylbenzenes. The reaction usually gave moderate yields and catalyst-dependent was seen in some cases. The reaction is compatible with other reported dipyrromethane syntheses and could be applied for the construction of unusual porphyrins. © 2008 Elsevier Ltd. All rights reserved. | * |
dc.language | English | * |
dc.title | Direct alkylation of pyrrole with vinyl substituted aromatics: versatile precursors for the synthesis of porphyrinoid macrocycles | * |
dc.type | Article | * |
dc.relation.issue | 26 | * |
dc.relation.volume | 49 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 4138 | * |
dc.relation.lastpage | 4141 | * |
dc.relation.journaltitle | Tetrahedron Letters | * |
dc.identifier.doi | 10.1016/j.tetlet.2008.04.119 | * |
dc.identifier.wosid | WOS:000256771400015 | * |
dc.identifier.scopusid | 2-s2.0-44149119018 | * |
dc.author.google | Hong S.-J. | * |
dc.author.google | Jeong S.-D. | * |
dc.author.google | Yoo J. | * |
dc.author.google | Kim J.S. | * |
dc.author.google | Yoon J. | * |
dc.author.google | Lee C.-H. | * |
dc.contributor.scopusid | 윤주영(7403587371) | * |
dc.date.modifydate | 20240118162450 | * |