胺-1a和-1b:通过整合NMR光谱分析,理论计算和总合成来阐明结构
Tomohiro Obana1, Miyu Nakajima1, Kazuki Nakazato1
1Department of Applied Chemistry, Faculty of Science and Engineering, Chuo University, 1-13-27 Kasuga, Bunkyo-ku, Tokyo 112-8551, Japan.
Journal of the American Chemical Society
|October 17, 2024
概括
已经确定了具有抗癌性质的海洋宏酸 - 1a的正确结构. 这项研究纠正了之前提出的结构,并澄清了相关化合物的立体化学.
科学领域:
- 海洋天然产品化学
- 有机合成
- 化学结构的阐明
背景情况:
- 伊利莫托利德-1a是一种对人类癌细胞有强大的细胞毒性作用的海洋宏.
- 提出的结构已经合成,但它的正确性仍不确定十多年.
- 阐明复杂的自然产品的精确立体化学对于理解它们的生物活性至关重要.
研究的目的:
- 为了确定基胺-1a的正确结构.
- 解决宏和侧链立体同位素的配置模两可.
- 通过总合成来确认结构,并确定同源基-1b的结构.
主要方法:
- 综合策略涉及NMR光谱分析和基于分子力学的结构分析,用于配置重新分配.
- 模型合成以验证宏拉克域的重新配置.
- 用GIAO的NMR计算和DP4+分析进行侧链的立体异构分化.
- 阐明的结构及其同类物-1b的总合成.
主要成果:
- 已经确定了基胺-1a的正确结构,纠正了之前提出的结构.
- 麦克罗拉克和侧链的立体化学被准确地分配.
- 同时还确定了天然同源基-1b的结构.
- 成功的总合成验证了拟议的结构.
结论:
- 这项研究提供了对Iriomoteolide-1a和Iriomoteolide-1b的正确结构分配.
- 将光谱,计算和合成方法结合在一起的综合方法在复杂的自然产品结构阐释中被证明是有效的.
- 这项研究阐明了菌素的细胞毒性作用的结构基础,有助于未来的药物开发工作.
相关概念视频
Regioselectivity and Stereochemistry of Hydroboration
8.1K
A significant aspect of hydroboration–oxidation is the regio- and stereochemical outcome of the reaction.
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
8.1K
¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons
1.5K
Replacing each alpha-hydrogen in chloroethane by bromine (or a different functional group) yields a pair of enantiomers. Such protons are called prochiral or enantiotopic and are related by a mirror plane. Enantiotopic protons are chemically equivalent in an achiral environment. Because most proton NMR spectra are recorded using achiral solvents, enantiotopic hydrogens yield a single signal.
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
1.5K
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
3.4K
The Hofmann and Curtius rearrangement reactions can be applied to synthesize primary amines from carboxylic acid derivatives such as amides and acyl azides. In the Hofmann rearrangement, a primary amide undergoes deprotonation in the presence of a base, followed by halogenation to generate an N-haloamide. A second proton abstraction produces a stabilized anionic species, which rearranges to an isocyanate intermediate via an alkyl group migration from the carbonyl carbon to the neighboring...
3.4K
Stereoisomerism of Cyclic Compounds
8.7K
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,...
8.7K
Indirect-Acting Cholinergic Agonists: Chemistry and Structure-Activity Relationship
534
Indirect-acting cholinergic agonists are agents that interact with the acetylcholinesterase enzyme in the synaptic cleft, preventing the breakdown of acetylcholine into choline and acetate. Consequently, the concentration of acetylcholine in the synaptic cleft increases. These agonists can be classified into reversible and irreversible inhibitors based on their duration of action.
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
Reversible inhibitors display short to medium durations of action. Short-acting agents include simple alcohols with...
534
Aromatic Hydrocarbon Anions: Structural Overview
2.7K
Neutral hydrocarbons like cyclopentadiene with an odd number of carbon atoms and one intervening CH2 group in the ring are not aromatic. Cyclopentadiene with 4 π electrons does not satisfy the 4n + 2 π electron rule. Additionally, the intervening CH2 group is sp3 hybridized and lacks a vacant p orbital, thereby interrupting the overlap of p orbitals in a continuous manner and preventing the delocalization of π electrons throughout the ring.
Due to the absence of continuous...
Due to the absence of continuous...
2.7K

![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)
