首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Towards the real didemnaketal A: total syntheses of two C-21 stereoisomers of the proposed didemnaketal A
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Towards the real didemnaketal A: total syntheses of two C-21 stereoisomers of the proposed didemnaketal A

机译:迈向真正的双锁链A:拟议的双锁链A的两个C-21立体异构体的总合成

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摘要

Two isomers (3 and 4) with a configuration at C-21 opposite to that proposed for didemnaketal A were synthesized through a process in which the longest linear sequence involved 29 steps. Comparative NMR analysis of these isomers and natural didemnaketal A suggests the possibility of misassignments at other stereocenters in the proposed structure of didemnaketal A
机译:通过最长线性序列涉及29个步骤的过程合成了两个异构体(3和4),其在C-21处的构型与对双母核A所提议的构型相反。对这些异构体和天然双半乳酮A进行的比较NMR分析表明,双半乳酮A拟议结构中其他立体中心存在错配的可能性

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