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Formal total synthesis of (+)-wortmannin using catalytic asymmetric intramolecular aldol condensation reaction

机译:催化不对称分子内羟醛缩合反应正式合成(+)-渥曼青霉素

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摘要

A catalytic process for the synthesis of optically active C4-substituted tetrahydroindandiones using an asymmetric intramolecular aldol condensation reaction was developed. When 30 mol% of phenylalanine and 50 mol% of pyridinium p-toluenesulfonate were used under highly concentrated conditions, a variety of C4-substituted tetrahydroindandiones and octahydronaphthalenediones were obtained in high yield (up to 89% yield) and high enantiomeric excess (up to 94% ee). One of the products was successfully transformed into the key intermediate for the synthesis of the phosphatidylinositol 3-kinase inhibitor wortmannin, achieving formal total synthesis of (+)-wortmannin. (c) 2005 Elsevier Ltd. All rights reserved.
机译:开发了使用不对称分子内羟醛缩合反应合成旋光C4取代的四氢茚二酮的催化方法。在高浓度条件下使用30摩尔%的苯丙氨酸和50摩尔%的对甲苯磺酸吡啶鎓时,可以高收率(最高收率89%)和高对映体过量(最高收率)获得各种C4取代的四氢茚二酮和八氢萘二酮。 94%ee)。其中一种产品已成功转化为合成磷脂酰肌醇3-激酶抑制剂渥曼青霉素的关键中间体,从而实现了(+)-渥曼青霉素的正式全合成。 (c)2005 Elsevier Ltd.保留所有权利。

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