通过NBS介导的N,N-二甲基胺的C-H化与N-酸胺的化
Shuangqing Li1, Xianru Xu1, Guojuan Yin1
1College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou 325035, China. xyz@wzu.edu.cn.
概括
这项研究引入了一种新的方法,通过NBS介导的C(sp3) -H键的化生成甲基二胺. 这种高效和多功能反应为合成各种胺化合物提供了实用方法.
科学领域:
- 有机化学 有机化学
- 合成方法论 合成方法论
- 催化剂是一种催化剂.
背景情况:
- C-H 键功能化是合成化学的一个关键领域.
- 化反应对于合成生物相关分子至关重要.
- 开发有效的C ((sp3) -H化方法仍然是一个挑战.
研究的目的:
- 开发一种新的NBS介导的化策略,用于相邻的C ((sp3) -H键.
- 通过使用N-acyloxyamides作为胺源合成多种类型的甲二胺.
- 探索开发的方法论的范围和局限性.
主要方法:
- 通过N-糖胺 (NBS) 介导的基质化.
- 使用N-酸胺作为高效的胺源.
- 反应条件的优化,以温和和高效.
主要成果:
- 在N,N-二甲基胺中,成功化原子旁边的C(sp3) -H键.
- 形成各种各样的甲二胺.
- 展示了卓越的功能组耐受性和高反应效率.
- 格拉姆尺度合成和易产品衍生证实了实用性.
结论:
- 开发的NBS介导的化物提供了一条有效的途径到甲二胺.
- 反应在温和条件下进行,具有广泛的功能组兼容性.
- 初步的机理学研究表明,这是一种激进交叉合的途径.
相关概念视频
¹³C NMR: ¹H–¹³C Decoupling
994
The probability of having two carbon-13 atoms next to each other is negligible because of the low natural abundance of carbon-13. Consequently, peak splitting due to carbon-carbon spin-spin coupling is not observed in spectra. However, protons up to three sigma bonds away split the carbon signal according to the n+1 rule, resulting in complicated spectra.
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
994
Nonsense-mediated mRNA Decay
10.4K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
10.4K
NMR Spectroscopy: Spin–Spin Coupling
1.2K
The spin state of an NMR-active nucleus can have a slight effect on its immediate electronic environment. This effect propagates through the intervening bonds and affects the electronic environments of NMR-active nuclei up to three bonds away; occasionally, even farther. This phenomenon is called spin–spin coupling or J-coupling. Coupling interactions are mutual and result in small changes in the absorption frequencies of both nuclei involved. While nuclei of the same element are involved...
1.2K
Spin–Spin Coupling Constant: Overview
862
In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
862
Spin–Spin Coupling: One-Bond Coupling
922
Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
922
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
942
Two NMR-active nuclei bonded to a central atom can be involved in geminal or two-bond coupling. Geminal coupling is commonly seen between diastereotopic protons in chiral molecules and unsymmetrical alkenes, among others.
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
942


