马鞭草甾体生物碱的战略汇聚合成途径

IF 4.6 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Chemistry Frontiers Pub Date : 2024-06-10 DOI:10.1039/D4QO00717D
Zhuo Wang
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引用次数: 0

摘要

马鞭草甾体生物碱是一种高度复杂的生物碱,具有连接到哌啶环的 C-nor-D-homo甾体骨架。受马鞭草甾体生物碱复杂结构和生物特性的吸引,2009 年通过半合成方法首次合成了环丙胺。最近,马鞭草甾体生物碱的合成以聚合方法为特色而蓬勃发展。在这篇高亮论文中,我们讨论了实现马鞭草甾体生物碱高官能化、复杂分子结构的合成策略,并强调了其中涉及的关键反应。我们重点介绍了马鞭草甾体生物碱的合成现状,并讨论了聚合合成法在复杂天然产物合成中的未来发展方向和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Strategic convergent synthesis en route to Veratrum steroidal alkaloids

Veratrum steroidal alkaloids are highly intricate alkaloids with a C-nor-D-homo steroid skeleton linked to a piperidine ring. These alkaloids have fascinated researchers due to their structural complexity and biological properties. The first synthesis of cyclopamine was accomplished in 2009 via a semi-synthetic approach. More recently, the synthesis of Veratrum steroidal alkaloids has made significant progress, employing a convergent approach. In this Highlight, we discuss the synthetic strategy that yields the highly functionalized, complex molecular architecture of Veratrum steroidal alkaloids, emphasizing key reactions involved. We also explore the current state of the synthesis of Veratrum steroidal alkaloids and discuss future directions and opportunities for the convergent synthetic approach in complex natural product synthesis.

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来源期刊
Organic Chemistry Frontiers
Organic Chemistry Frontiers CHEMISTRY, ORGANIC-
CiteScore
7.90
自引率
11.10%
发文量
686
审稿时长
1 months
期刊介绍: Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.
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