相关实验视频
Updated: Jul 8, 2026
![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)
05:15
Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
盐酸乙烯酸乙胺宏化物氧米丁II的总合成
1Department of Chemistry and Center for Chemical Methodology and Library Development, Boston University, 590 Commonwealth Avenue, Massachusetts 02215, USA.
Journal of the American Chemical Society
|June 6, 2003
概括
研究人员报告了氧化二胺二的不对称合成,这是一个酸盐胺宏化物. 这项研究突出了用于宏循环结构的立体选择性环闭元解和用于侧链附着的铜介导化.
科学领域:
- 有机化学 有机化学
- 宏类合成 宏类合成
- 不对称的合成方法
背景情况:
- 酸盐酶胺宏化物是具有潜在生物活性的复杂自然产品.
- 氧化二胺是该类中一个特定的目标,需要复杂的合成策略.
研究的目的:
- 为了开发一种高效的不对称合成的oximidine II大化物.
- 建立一个可靠的方法来构建宏环三烯核心,并连接胺侧链.
主要方法:
- 不对称合成利用 bis-diene基质的环闭转化 (RCM).
- 区域和立体选择性RCM形成宏环三烯核.
- 一个 (Z) - 乙化的铜 (I) - 催化化,用于化侧链装置.
主要成果:
- 成功构建了具有高区域和立体选择性的宏环三烯核.
- 通过铜 (I) 介导的化剂有效地连接化物侧链.
- 证明一种可行的合成路径到氧米丁II.
结论:
- 报告的合成策略为oximidine II提供了一条新的途径.
- 使用的方法适用于合成其他复杂的宏类化合物.
- 这项工作推进了不对称的宏化物合成领域.
相关概念视频
Conjugate Addition of Enolates: Michael Addition
The attack of a nucleophile at the β carbon of an α,β-unsaturated carbonyl compound is called conjugate addition. Conjugate addition reactions of active methylene compounds, such as β-diketones, β-keto esters, β-keto nitriles, and α-nitro ketones, are called Michael addition reactions.
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Acetoacetic ester synthesis is a method to obtain ketones from alkyl halides and β-keto esters. The reaction occurs in the presence of an alkoxide base that abstracts the acidic proton of the β-keto esters. The step results in an enolate ion which is doubly stabilized. The enolate then reacts with an alkyl halide via the SN2 process to produce an alkylated ester intermediate with a new C–C bond. The hydrolysis of the intermediate, followed by acidification, results in an alkylated β-keto acid.
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.
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).
Combined Effects of Drugs: Synergism
Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
Such synergistic combinations...

