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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >The first stereoselective total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-α-pyranone and total synthesis of (2S,3K,5S)-(-)-2,3-dihydroxytetradecan-5-olide
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The first stereoselective total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-α-pyranone and total synthesis of (2S,3K,5S)-(-)-2,3-dihydroxytetradecan-5-olide

机译:(3S,4R)-二羟基-(6S)-十一烷基-α-吡喃酮的全立体选择性全合成和(2S,3K,5S)-(-)-2,3-二羟基十四烷-5-油化物的全合成

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摘要

The first total synthesis of (3S,4R)-dihydroxy-(6S)-undecyl-α-pyranone 1 and total synthesis of (2S,3R,5S)-(-)-2,3-dihydroxytetradecan-5-olide 2 have been achieved in five steps in a highly stereoselective manner using Maruoka aliylation, olefin cross-metathesis, and Sharpless asymmetric dihydroxylation as key steps.
机译:(3S,4R)-二羟基-(6S)-十一烷基-α-吡喃酮1的首次全合成和(2S,3R,5S)-(-)-2,3-二羟基十四烷-5-醇化物2的全合成以Maruoka酰化,烯烃交叉复分解和Sharpless不对称二羟基化为关键步骤,以高度立体选择性的方式通过五个步骤实现了这一目标。

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