First total synthesis of murisolin

The first and concise total synthesis of murisolin (1) was accomplished using asymmetric alkynylation and Sonogashira coupling as the key steps. The threo/trans/threo-type THF ring moiety was constructed with excellent stereoselectivity by asymmetric alkynylation of 1,6-heptadiyne to alpha-tetrahydr...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2004-02 (4), p.406-407
Hauptverfasser: Maezaki, Naoyoshi, Tominaga, Hiroaki, Kojima, Naoto, Yanai, Minori, Urabe, Daisuke, Tanaka, Tetsuaki
Format: Artikel
Sprache:eng
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Zusammenfassung:The first and concise total synthesis of murisolin (1) was accomplished using asymmetric alkynylation and Sonogashira coupling as the key steps. The threo/trans/threo-type THF ring moiety was constructed with excellent stereoselectivity by asymmetric alkynylation of 1,6-heptadiyne to alpha-tetrahydrofuranic aldehyde, which was also prepared via the asymmetric alkynylation.
ISSN:1359-7345
DOI:10.1039/b312362f