Tropane衍生物的合成

Abdulmajeed S H Alsamarrai
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引用次数: 0

摘要

本章是指在茄科植物的一个分支中,包括Atropa、Duboisia、Hyoscyamus和Scopolia物种,以及它们的半合成衍生物中,以其存在、生物合成和药理特性而闻名的莨菪烷生物碱化合物。Tropane生物碱是有用的副交感神经抑制剂,竞争性拮抗乙酰胆碱。这些生物碱的碱是由tropane部分的双环构成的,大部分tropane生物碱以酯衍生物的形式被取代在tropane环的C-3原子上。此外,本章还提供了之前合成2-托帕-2-基衍生物的方法路线,以及合成2-(对甲苯磺基)托帕-2-烯(无氢ecgonine)的新路线。这一新的合成策略可能有助于采用最佳的方法合成tropane-2-yl衍生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of Tropane Derivatives
This chapter refers to tropane alkaloid compounds best known for their occurrence, biosynthesis, and pharmacological properties in a subsection of the plant family Solanaceae including the Atropa , Duboisia , Hyoscyamus , and Scopolia species, together with their semisynthetic derivatives. Tropane alkaloids are useful as parasympatholytics that competitively antagonize acetylcholine. The bicyclic ring of tropane moiety forms the base of these alkaloids, and the largest number of tropane alkaloids is substituted on the atom C-3 of the tropane ring in the form of ester derivatives. Also, this chapter provides routes to previous methods for synthesizing tropane-2-yl derivatives as well as new routes to synthesize 2-( p -toluenesulphonyl) tropane-2-ene (anhydroecgonine). The new strategy for synthesizing anhydroecgonine might be helpful to adopt the best method of synthesizing tropane-2-yl derivatives.
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