立体特异性合物功能化:合物复合物与电友的反应
Cristina García-Ruiz1, Jack L-Y Chen1, Christopher Sandford1
1School of Chemistry, University of Bristol , Cantock's Close, Bristol BS8 1TS, United Kingdom.
Journal of the American Chemical Society
|October 14, 2017
概括
由酸激活的酸复合物对各种电友的反应性大大增强. 这一突破使得具有新功能和立体中心的复杂分子能够高效合成.
科学领域:
- 有机金属化学
- 合成有机化学
背景情况:
- 乙烯 Ester 是已知的核爱体,主要与碳基和胺基反应.
- 它们的反应性仅限于更广泛的电友物种.
研究的目的:
- 为了增强基的核友性.
- 扩大与烯酸试剂反应的电友的范围.
- 开发一种高立体控制的功能化分子合成的新方法.
主要方法:
- 使用酸试剂激活酸以形成酸复合物.
- 激活复合物的反应与各种电友,包括,二,激活,埃申莫瑟盐,托尼试剂,Selectfluor,二二碳酸盐 (DIAD) 和MeSX.
- 对反应产物的区域和立体化学结果的分析.
主要成果:
- 酸复合物显著增强核友性,比原始酸大7到10个数量级.
- 通过高区域和立体控制,成功添加了广泛的电友.
- 该协议提供了新的功能,包括具有和三甲基的四级立体中心.
结论:
- 通过阿里利介导的激活显著增加了基的反应性.
- 这种方法为复杂有机分子的立体选择性合成提供了一种多功能且强大的方法.
- 开发的协议扩大了在有机化学中的合成试剂的用途.
相关概念视频
Metal-Ligand Bonds
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
Valence Bond Theory
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
Thermal Electrocyclic Reactions: Stereochemistry
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Cycloaddition Reactions: MO Requirements for Thermal Activation
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
Complexation Equilibria: The Chelate Effect
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
Complexation Equilibria: Factors Influencing Stability of Complexes
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...


