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不对称的 (-) - 昆诺的总合成
Yan-Chao Wu1, Mélanie Liron, Jieping Zhu
1Institut de Chimie des Substances Naturelles, CNRS, 91198 Gif-sur-Yvette Cedex, France.
Journal of the American Chemical Society
|May 6, 2008
概括
在22个步骤中实现了 (-) - 奎诺卡辛的总合成. 关键步骤包括皮克特-斯潘格勒反应和白银催化曼尼赫反应,以构建复杂的五环结构.
科学领域:
- 有机化学 有机化学
- 合成化学 合成化学
背景情况:
- (-) - - 昆诺卡辛是一种复杂的五环天然产品.
- 以前的合成路线是有限的或不完整的.
研究的目的:
- 为了实现 (-) - 基诺卡辛的总合成.
- 开发用于复杂分子构造的新型合成方法.
主要方法:
- 一个22步线性合成,从3-基甲开始.
- 利用皮克特-斯潘格勒反应来形成四化诺.
- 采用白银催化的分子内曼尼赫反应来构建二氧化[3,2,1]-八度核.
主要成果:
- 在 (-) - - 昆诺卡辛的整体收益率为16%.
- 皮克特-斯潘格勒反应只能 (91%) 产生所需的1,3-cis立体异构体.
- 开发了一种新的Hf(OTf) 4-催化转化aminal到氨基 thioether.
结论:
- (-) - - 奎诺卡辛的总合成成功完成.
- 开发的合成策略适用于其他复杂的自然产品.
- 该研究强调了特定反应条件对于具有挑战性的循环化的重要性.
相关概念视频
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Malonic ester synthesis is a method to obtain α substituted carboxylic acids from ꞵ-diesters such as diethyl malonate and alkyl halides.
Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents
Carboxylic acids can be prepared by the carboxylation of Grignard reagents (RMgX). This method is convenient for converting alkyl (primary, secondary or tertiary), vinyl, benzyl, and aryl halides to carboxylic acids with one additional carbon than the starting RMgX.
Preparation of Carboxylic Acids: Overview
There are various methods for the preparation of carboxylic acids. For example, oxidation of primary alcohols or aldehydes using strong oxidizing agents results in a carboxylic acid. Aldehydes can also be oxidized in the presence of mild oxidizing agents.
Preparation of 1° Amines: Azide Synthesis
Direct alkylation of ammonia produces polyalkylated amines, along with a quaternary ammonium salt. To exclusively prepare primary amines, the azide synthesis method can be used.
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation
Robinson annulation is a base-catalyzed reaction for the synthesis of 2-cyclohexenone derivatives from 1,3-dicarbonyl donors (such as cyclic diketones, β-ketoesters, or β-diketones) and α,β-unsaturated carbonyl acceptors. Named after Sir Robert Robinson, who discovered it, this reaction yields a six-membered ring with three new C–C bonds (two σ bonds and one π bond).
Preparation of Amides
Amides are synthesized by treating carboxylic acids with amines in the presence of dehydrating agents like dicyclohexylcarbodiimide (DCC).
The DCC-promoted synthesis of amides begins with the protonation of DCC by carboxylic acid. The protonation makes it a better acceptor. Next, the addition of carboxylate to the protonated carbodiimide gives a reactive acylating agent.
Subsequently, the amine acts as a nucleophile that attacks the acylating agent to form a tetrahedral intermediate. In the...
The DCC-promoted synthesis of amides begins with the protonation of DCC by carboxylic acid. The protonation makes it a better acceptor. Next, the addition of carboxylate to the protonated carbodiimide gives a reactive acylating agent.
Subsequently, the amine acts as a nucleophile that attacks the acylating agent to form a tetrahedral intermediate. In the...

