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A biocatalytic hydroxylation-enabled unified approach to C19-hydroxylated steroids

机译:C19-羟基化类固醇的生物催化羟基化启用统一方法

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摘要

Steroidal C19-hydroxylation is pivotal to the synthesis of naturally occurring bioactive C19-OH steroids and 19-norsteroidal pharmaceuticals. However, realizing this transformation is proved to be challenging through either chemical or biological synthesis. Herein, we report a highly efficient method to synthesize 19-OH-cortexolone in 80% efficiency at the multi-gram scale. The obtained C19-OH-cortexolone can be readily transformed to various synthetically useful intermediates including the industrially valuable 19-OH-androstenedione, which can serve as a basis for synthesis of C19-functionalized steroids as well as 19-nor steroidal drugs. Using this biocatalytic C19-hydroxylation method, the unified synthesis of six C19-hydroxylated pregnanes is achieved in just 4 to 9 steps. In addition, the structure of sclerosteroid B is revised on the basis of our synthesis.
机译:甾体C19-羟基化对于合成天然存在的生物活性C19-OH类固醇和19-甾体类药物至关重要。然而,通过化学或生物合成证明实现这种转化是具有挑战性的。在这里,我们报告了一种高效的方法,可以在多克规模下以80%的效率合成19-OH-皮质酮。所获得的C19-OH-皮质酮可以容易地转化为各种合成有用的中间体,包括工业上有价值的19-OH-雄烯二酮,其可以用作合成C19-官能化的类固醇以及19-非甾体类药物的基础。使用这种生物催化的C19-羟基化方法,仅需4到9个步骤即可完成6个C19-羟基化孕烷的统一合成。另外,硬化甾体B的结构根据我们的合成进行了修改。

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