Catalytic enantioselective bromolactonization of alkenoic acids in the presence of palladium complexes
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, Hyun Joo | - |
dc.contributor.author | Kim, Dae Young | - |
dc.date.accessioned | 2021-08-12T02:25:34Z | - |
dc.date.available | 2021-08-12T02:25:34Z | - |
dc.date.issued | 2012-12-19 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/14592 | - |
dc.description.abstract | The catalytic enantioselective bromolactonization of alkenoic acids promoted by chiral palladium complexes has been developed, allowing facile synthesis of the corresponding gamma-lactones with excellent enantioselectivity (up to 97% ee). The method reported represents a practical entry for the preparation of chiral gamma-lactone derivatives. (C) 2012 Elsevier Ltd. All rights reserved. | - |
dc.format.extent | 3 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Elsevier BV | - |
dc.title | Catalytic enantioselective bromolactonization of alkenoic acids in the presence of palladium complexes | - |
dc.type | Article | - |
dc.publisher.location | 영국 | - |
dc.identifier.doi | 10.1016/j.tetlet.2012.10.051 | - |
dc.identifier.scopusid | 2-s2.0-84869206445 | - |
dc.identifier.wosid | 000312231400029 | - |
dc.identifier.bibliographicCitation | Tetrahedron Letters, v.53, no.51, pp 6984 - 6986 | - |
dc.citation.title | Tetrahedron Letters | - |
dc.citation.volume | 53 | - |
dc.citation.number | 51 | - |
dc.citation.startPage | 6984 | - |
dc.citation.endPage | 6986 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | sci | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | MANNICH-TYPE REACTIONS | - |
dc.subject.keywordPlus | BETA-KETO-ESTERS | - |
dc.subject.keywordPlus | ELECTROPHILIC ALPHA-AMINATION | - |
dc.subject.keywordPlus | FRIEDEL-CRAFTS ALKYLATION | - |
dc.subject.keywordPlus | CONJUGATE ADDITION | - |
dc.subject.keywordPlus | ASYMMETRIC BROMOLACTONIZATION | - |
dc.subject.keywordPlus | ALPHA,BETA-UNSATURATED KETONES | - |
dc.subject.keywordPlus | FUMARATE DERIVATIVES | - |
dc.subject.keywordPlus | MICHAEL ADDITION | - |
dc.subject.keywordPlus | FLUORINATION | - |
dc.subject.keywordAuthor | Asymmetric catalysis | - |
dc.subject.keywordAuthor | Chiral palladium catalysts | - |
dc.subject.keywordAuthor | Bromolactonization | - |
dc.subject.keywordAuthor | gamma-Lactones | - |
dc.subject.keywordAuthor | Alkenoic acids | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
(31538) 22, Soonchunhyang-ro, Asan-si, Chungcheongnam-do, Republic of Korea+82-41-530-1114
COPYRIGHT 2021 by SOONCHUNHYANG UNIVERSITY ALL RIGHTS RESERVED.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.