Expedient synthesis of 4-O-methylhonokiol via Suzuki-Miyaura cross-coupling
DC Field | Value | Language |
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dc.contributor.author | Kwak, Jae-Hwan | - |
dc.contributor.author | Cho, Young Ae | - |
dc.contributor.author | Jang, Jae-Yong | - |
dc.contributor.author | Seo, Seung-Yong | - |
dc.contributor.author | Lee, Heesoon | - |
dc.contributor.author | Hong, Jin Tae | - |
dc.contributor.author | Han, Sang-Bae | - |
dc.contributor.author | Lee, Kiho | - |
dc.contributor.author | Kwak, Young-Shin | - |
dc.contributor.author | Jung, Jae-Kyung | - |
dc.date.accessioned | 2021-09-07T05:17:54Z | - |
dc.date.available | 2021-09-07T05:17:54Z | - |
dc.date.created | 2021-06-18 | - |
dc.date.issued | 2011-12-02 | - |
dc.identifier.issn | 0040-4020 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/110926 | - |
dc.description.abstract | Concise and practical synthesis of 4-O-methylhonokiol was achieved in 34% overall yield. The key features of our synthesis include chemoselective ortho-mono bromination of phenol as well as biaryl formation via Suzuki-Miyaura cross-coupling, in which bromophenol was reacted with potassium aryltrifluoroborate using Pd(OAc)(2) and RuPhos under microwave conditions. (C) 2011 Elsevier Ltd. All rights reserved. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.subject | CONCISE SYNTHESIS | - |
dc.subject | NEOLIGNANS | - |
dc.subject | ACIDS | - |
dc.title | Expedient synthesis of 4-O-methylhonokiol via Suzuki-Miyaura cross-coupling | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, Kiho | - |
dc.contributor.affiliatedAuthor | Kwak, Young-Shin | - |
dc.identifier.doi | 10.1016/j.tet.2011.09.115 | - |
dc.identifier.scopusid | 2-s2.0-80054850043 | - |
dc.identifier.wosid | 000297444100020 | - |
dc.identifier.bibliographicCitation | TETRAHEDRON, v.67, no.48, pp.9401 - 9404 | - |
dc.relation.isPartOf | TETRAHEDRON | - |
dc.citation.title | TETRAHEDRON | - |
dc.citation.volume | 67 | - |
dc.citation.number | 48 | - |
dc.citation.startPage | 9401 | - |
dc.citation.endPage | 9404 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | CONCISE SYNTHESIS | - |
dc.subject.keywordPlus | NEOLIGNANS | - |
dc.subject.keywordPlus | ACIDS | - |
dc.subject.keywordAuthor | Neolignan | - |
dc.subject.keywordAuthor | 4-O-Methylhonokiol | - |
dc.subject.keywordAuthor | Suzuki-Miyaura cross-coupling | - |
dc.subject.keywordAuthor | Potassium aryltrifluoroborate | - |
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