Photoinduced Transition-Metal-Free Cross-Coupling of Aryl Halides with H-Phosphonates
作者:Huiying Zeng、Qian Dou、Chao-Jun Li
DOI:10.1021/acs.orglett.8b04081
日期:2019.3.1
Photoinduced transition-metal- and photosensitizer-free cross-coupling of arylhalides (including Ar–Cl, Ar–Br, and Ar–I) with H-phosphonates (including dialkyl phosphonates and diarylphosphine oxides) is reported. Various functional groups were tolerated, including ester, methoxy, dimethoxy, alkyl, phenyl, trifluoromethyl, and heterocyclic compounds. This simple and green strategy provides a practical
Visible-Light-Induced Nickel-Catalyzed P(O)–C(sp<sup>2</sup>) Coupling Using Thioxanthen-9-one as a Photoredox Catalysis
作者:Da-Liang Zhu、Shan Jiang、Qi Wu、Hao Wang、Lu-Lu Chai、Hai-Yan Li、Hong-Xi Li
DOI:10.1021/acs.orglett.0c03892
日期:2021.1.1
developed for photocatalytic P(O)–C(sp2) coupling of (hetero)aryl halides with H-phosphine oxides or H-phosphites under the irradiation of visible light or sunlight. The thioxanthen-9-one/nickel dual catalysis mediates this phosphonylation to give arylphosphine oxides and arylphosphonates in moderate to excellent yields. This transformation is widely tolerant to a range of functional groups and proceeds
A simple azine-linked covalent organic framework (COF) with high thermal and chemical stabilities has been prepared by using deep eutectic solvent (DES) as green media. The as-synthesized COF was employed as heterogeneous ligand for immobilization of PdII. The obtained Pd-supported COF nanoparticles catalyst (defined as Pd/TFPT-Azine-COF) was found to be an efficient heterogeneouscatalyst for the
This work describes a straightforward access to a large variety of arylphosphonates by the simple combination of diaryliodonium salts with phosphites in the presence of a base and under visible-light illumination. The reaction proceeds smoothly, tolerates various functionalities, and was applied for the synthesis of pharmaceutically relevant compounds. Mechanistic investigations, including EPR, NMR
Structural modification and the coronaryvasodilator activity of the calcium antagonist fostedil (KB-944) are described. Elimination of the bezothiazole ring or replacement of the benzothiazole ring of fostedil with other hetero rings leads to a decrease in vasodilator activity. Change of the distance from the aromatic ring to the phosphorus of fostedil causes a decrease in the activity. The present