Palladium(II)-Catalyzed Tandem Synthesis of Acenes Using Carboxylic Acids as Traceless Directing Groups
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kiho Kim | - |
dc.contributor.author | Dhananjayan Vasu | - |
dc.contributor.author | Honggu Im | - |
dc.contributor.author | Sungwoo Hong | - |
dc.date.available | 2018-07-18T02:09:29Z | - |
dc.date.created | 2018-03-16 | - |
dc.date.issued | 2016-07 | - |
dc.identifier.issn | 1433-7851 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/4835 | - |
dc.description.abstract | A straightforward synthetic strategy for generating useful anthracene derivatives was developed involving palladium(II)-catalyzed tandem transformation with carboxylic acids as traceless directing groups. Carboxyl-directed C-H alkenylation, carboxyl-directed secondary C-H activation and rollover, intramolecular C-C bond formation, and decarboxylative aromatization are proposed as the key steps in the tandem reaction pathway. This novel synthetic route utilizes a broad range of substrates and provides a convenient synthetic tool that allows access to acenes (c) 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.subject | acenes | - |
dc.subject | C-H functionalization | - |
dc.subject | decarboxylation | - |
dc.subject | palladium | - |
dc.subject | tandem reactions | - |
dc.title | Palladium(II)-Catalyzed Tandem Synthesis of Acenes Using Carboxylic Acids as Traceless Directing Groups | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000383253500029 | - |
dc.identifier.scopusid | 2-s2.0-84973092387 | - |
dc.identifier.rimsid | 62506 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Kiho Kim | - |
dc.contributor.affiliatedAuthor | Dhananjayan Vasu | - |
dc.contributor.affiliatedAuthor | Honggu Im | - |
dc.contributor.affiliatedAuthor | Sungwoo Hong | - |
dc.identifier.doi | 10.1002/anie.201603661 | - |
dc.identifier.bibliographicCitation | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.55, no.30, pp.8652 - 8655 | - |
dc.citation.title | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
dc.citation.volume | 55 | - |
dc.citation.number | 30 | - |
dc.citation.startPage | 8652 | - |
dc.citation.endPage | 8655 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 16 | - |
dc.description.scptc | 15 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | H BOND ACTIVATION | - |
dc.subject.keywordPlus | POLYCYCLIC AROMATIC-COMPOUNDS | - |
dc.subject.keywordPlus | DIELS-ALDER REACTIONS | - |
dc.subject.keywordPlus | C-H | - |
dc.subject.keywordPlus | BENZOIC-ACIDS | - |
dc.subject.keywordPlus | DIRECT ARYLATION | - |
dc.subject.keywordPlus | PALLADIUM | - |
dc.subject.keywordPlus | CATALYSIS | - |
dc.subject.keywordPlus | CYCLIZATION | - |
dc.subject.keywordPlus | FUNCTIONALIZATION | - |
dc.subject.keywordAuthor | acenes | - |
dc.subject.keywordAuthor | C-H functionalization | - |
dc.subject.keywordAuthor | decarboxylation | - |
dc.subject.keywordAuthor | palladium | - |
dc.subject.keywordAuthor | tandem reactions | - |