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Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
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通过激素介导的三组件合和7-endo循环实现的树脂素的总合成
Satoshi Hashimoto1, Shun-Ichiro Katoh1, Takehiro Kato1
1Graduate School of Pharmaceutical Sciences, The University of Tokyo , Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
Journal of the American Chemical Society
|October 19, 2017
概括
这项研究提出了一种基于激素的新策略,用于合成一种强大的TRPV1激动剂树脂毒素. 这种新方法有效地构建了复杂的三环核,为复杂分子合成提供了多功能方法.
科学领域:
- 有机化学
- 合成化学
- 医学化学
背景情况:
- 树脂毒素 (1) 是一种具有强烈的对TRPV1的激活作用的达芬酸二,TRPV1是关键的疼痛和热传感器.
- 高氧化转5/7/6三碳循环核的树脂毒素提出了重要的合成挑战.
- 目前的合成策略在有效组装这些复杂的分子架构方面是有限的.
研究的目的:
- 开发一种基于基因的全合成树脂毒素的新方法 (1).
- 证明激素反应在复杂的碳循环系统中构建阻碍键的实用性.
- 为复杂自然产品的多步定向合成提供新的战略设计.
主要方法:
- 采用了三组分策略,包括A环,基和C环碎片.
- 第一个激素反应产生了A和C环的顺序合的α-基桥头激素.
- 第二个激素反应实现了7个成员的B环循环,立体中心结构和烯安装.
主要成果:
- 已经成功组装了氧化密度高的5/7/6三碳循环.
- 有效形成的激进策略阻碍了C9,10链接,并立体选择性地扩展了C4链.
- 通过高度优化的化学选择性转换,合成产生了树脂毒素.
结论:
- 开发的基于激素的策略为合成树脂毒素提供了一种高效和多功能方法.
- 这种方法突出了激素反应在没有功能组损伤的情况下构建复杂的碳循环的优势.
- 该战略为设计针对复杂分子的多步合成提供了一个新范式.
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