对称性驱动的氨醇总合成
Jake M Aquilina1, Myles W Smith1
1Department of Biochemistry, UT Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, Texas 75390, United States.
Journal of the American Chemical Society
|June 14, 2022
概括
这项研究首次对复杂的天然产物尿素进行了不对称的总合成. 这种新的策略利用隐藏的对称性和关键的脱对称化步骤来建立多个立体中心,包括四元中心.
科学领域:
- 有机化学
- 自然产品合成
- 医学化学
背景情况:
- 氨酸是一种具有潜在生物活性的天然产品.
- 复杂的类化合物如氨醇的总合成具有重大化学挑战.
- 现有的合成途径对尿素是有限的或缺乏立体化学控制.
研究的目的:
- 开发一种新且高效的全合成天然产品 - - 氨酸.
- 通过控制绝对立体化学, 建立了第一个非对称的神经尿素合成.
- 探索创新的合成策略,包括发现隐藏的对称性.
主要方法:
- 使用对称的二 precursor 的氨酸的总合成.
- 通过使用廉价的奇拉胺进行双重还原性氨化进行关键脱对称.
- 作为潜伏的cis-1,3-bis ((hydroxymethyl) 合成体的双环的战略使用.
- 用于立体化学控制的拓控制化.
主要成果:
- 实现了第一个非对称的肌尿醇全合成.
- 在绝对意义上成功建立了四个立体中心,包括核心四级立体中心.
- 合成涉及商业材料的18个步骤,总产量约为1%.
- 展示了一种利用多环结构中隐藏的对称性的新合成策略.
结论:
- 开发的合成途径提供了有效的立体选择性进入尿素.
- 该战略强调了在复杂分子合成中识别和利用隐藏的对称性的实用性.
- 这项工作为进一步探索氨醇类型及其潜在应用铺平了道路.
相关概念视频
Stereoisomerism of Cyclic Compounds
9.2K
In this lesson, we delve into the role of ring conformation and its stability, which determines the spatial arrangement and, consequently, the molecular symmetry and stereoisomerism of cyclic compounds. 1,2-Dimethylcyclohexane is used as a case study to evaluate the possible number of stereoisomers. Here, given the multiple (n = 2) chiral centers, there are 2n = 4 possible configurations that lack a plane of symmetry, as the ring skeleton exists in a non-planar chair conformation. In addition,...
9.2K
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation
2.3K
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).
2.3K
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
3.3K
Electrocyclic reactions, cycloadditions, and sigmatropic rearrangements are concerted pericyclic reactions that proceed via a cyclic transition state. These reactions are stereospecific and regioselective. The stereochemistry of the products depends on the symmetry characteristics of the interacting orbitals and the reaction conditions. Accordingly, pericyclic reactions are classified as either symmetry-allowed or symmetry-forbidden. Woodward and Hoffmann presented the selection criteria for...
3.3K
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
2.8K
The Cope rearrangement is classified as a [3,3] sigmatropic shift in 1,5-dienes, leading to a more stable, isomeric 1,5-diene. The reaction involves a concerted movement of six electrons, four from two π bonds and two from a σ bond, via an energetically favorable chair-like transition state.
2.8K
Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction
3.5K
α-Substituted ketones or aldehydes can be synthesized from enamines by the Stork enamine reaction, named after its pioneer Gilbert Stork. Enamines are useful synthetic intermediates where the lone pair on nitrogen is in conjugation with the C=C bond. They resemble enolate ions, as the resonance forms of both species have a nucleophilic α carbon.
3.5K
Biosynthesis of Lipids
91
Microbial membranes exhibit remarkable diversity in lipid composition, reflecting evolutionary adaptations to various environmental conditions. The three domains of life—Bacteria, Archaea, and Eukarya—synthesize membrane lipids through distinct biosynthetic pathways, leading to fundamental structural differences that impact membrane stability, function, and adaptability.Fatty Acid-Based Lipids in Bacteria and EukaryaBacteria and eukaryotes share a common fatty acid biosynthesis...
91

![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)
