Asymmetric Synthesis of (+)-trans-Aerangis Lactone
Asymmetric synthesis of (+)-trans-aerangis lactone was achieved from commercially available 1-hexanol or 1-hexanal in four steps via iridium-catalyzed diastereoselective and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level, and ruthenium-catalyzed olefin metathesis....
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Veröffentlicht in: | Bulletin of the Korean Chemical Society 2013, 34(1), , pp.75-78 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Asymmetric synthesis of (+)-trans-aerangis lactone was achieved from commercially available 1-hexanol or 1-hexanal in four steps via iridium-catalyzed diastereoselective and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level, and ruthenium-catalyzed olefin metathesis. KCI Citation Count: 6 |
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ISSN: | 0253-2964 1229-5949 |
DOI: | 10.5012/bkcs.2013.34.1.75 |