Total synthesis of daurichromenic acid
    1.
    发明授权
    Total synthesis of daurichromenic acid 失效
    总黄酮酸的合成

    公开(公告)号:US07102020B2

    公开(公告)日:2006-09-05

    申请号:US10739882

    申请日:2003-12-18

    Abstract: The present invention provides a method to prepare 2H-benzo[6]pyrans, such as the anti-HIV natural product daurichromenic acid (1a), by microwave-assisted tandem aldol reaction of a phenolic enolate followed by intramolecular SN2′ type cyclization to form the 2H-benzo[6]pyran core structure.

    Abstract translation: 本发明提供通过酚类烯醇化物的微波辅助串联醛醇缩合反应制备2H-苯并[6]吡喃如抗HIV天然产物多金红霉酸(1a)的方法,接着分子内SN2'型环化形成 2H-苯并[6]吡喃核心结构。

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