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An Optimized and General Synthetic Strategy To Prepare Arylnaphthalene Lactone Natural Products from Cyanophthalides
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Taejung | - |
| dc.contributor.author | Jeong, Kyu Hyuk | - |
| dc.contributor.author | Kang, Ki Sung | - |
| dc.contributor.author | Nakata, Masaya | - |
| dc.contributor.author | Ham, Jungyeob | - |
| dc.date.available | 2020-02-27T18:44:33Z | - |
| dc.date.created | 2020-02-06 | - |
| dc.date.issued | 2017-04-03 | - |
| dc.identifier.issn | 1434-193X | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/6211 | - |
| dc.description.abstract | A simple method for the preparation of arylnaphthalene lactone natural products was developed and used to synthesize diphyllin (10), justicidin A (12), cilinaphthalide B (13), taiwanin E (15), chinensinaphthol (16), taiwanin E methyl ether (17), chinensinaphthol methyl ether (18), justicidin C (21), and justicidin D (22). Key steps of the syntheses include the Hauser-Kraus annulation of cyanophthalides 7a and 7b and Suzuki-Miyaura cross-coupling reactions between arylnaphthalene lactones that contain a sulfonate group (i.e., 9, 14, 19, and 20) and various potassium aryltrifluoroborates. | - |
| dc.language | 영어 | - |
| dc.language.iso | en | - |
| dc.publisher | WILEY-V C H VERLAG GMBH | - |
| dc.relation.isPartOf | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | - |
| dc.subject | CROSS-COUPLING REACTIONS | - |
| dc.subject | JUSTICIA-PROCUMBENS | - |
| dc.subject | 1-ARYLNAPHTHALENE LIGNAN | - |
| dc.subject | PHYLLANTHUS-MYRTIFOLIUS | - |
| dc.subject | BIOLOGICAL EVALUATION | - |
| dc.subject | DERIVATIVES | - |
| dc.subject | ANALOGS | - |
| dc.subject | BIOEVALUATION | - |
| dc.subject | NEOLIGNANS | - |
| dc.subject | INHIBITORS | - |
| dc.title | An Optimized and General Synthetic Strategy To Prepare Arylnaphthalene Lactone Natural Products from Cyanophthalides | - |
| dc.type | Article | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.identifier.wosid | 000398575300003 | - |
| dc.identifier.doi | 10.1002/ejoc.201601611 | - |
| dc.identifier.bibliographicCitation | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, no.13, pp.1704 - 1712 | - |
| dc.identifier.scopusid | 2-s2.0-85017154457 | - |
| dc.citation.endPage | 1712 | - |
| dc.citation.startPage | 1704 | - |
| dc.citation.title | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | - |
| dc.citation.number | 13 | - |
| dc.contributor.affiliatedAuthor | Kang, Ki Sung | - |
| dc.type.docType | Article | - |
| dc.subject.keywordAuthor | Total synthesis | - |
| dc.subject.keywordAuthor | Natural products | - |
| dc.subject.keywordAuthor | Annulation | - |
| dc.subject.keywordAuthor | Cross-coupling | - |
| dc.subject.keywordAuthor | Lactones | - |
| dc.subject.keywordPlus | CROSS-COUPLING REACTIONS | - |
| dc.subject.keywordPlus | JUSTICIA-PROCUMBENS | - |
| dc.subject.keywordPlus | 1-ARYLNAPHTHALENE LIGNAN | - |
| dc.subject.keywordPlus | PHYLLANTHUS-MYRTIFOLIUS | - |
| dc.subject.keywordPlus | BIOLOGICAL EVALUATION | - |
| dc.subject.keywordPlus | DERIVATIVES | - |
| dc.subject.keywordPlus | ANALOGS | - |
| dc.subject.keywordPlus | BIOEVALUATION | - |
| dc.subject.keywordPlus | NEOLIGNANS | - |
| dc.subject.keywordPlus | INHIBITORS | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
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Related Researcher
- Kang, Ki Sung
- College of Korean Medicine (Premedical course of Oriental Medicine)