1608124-60-2

Upstream product

• 221044-05-9 N-(2-pyrimidyl)indole 
• 17873-01-7 (4-methylphenyl)trimethoxysilane 
• 1427669-82-6 (1-(pyrimidin-2-yl)-1H-indol-2-yl)(p-tolyl)methanone 
• 120-72-9 indole 
• 5720-05-8 4-methylphenylboronic acid 
• 99-94-5 p-Toluic acid 
• 18412-57-2 p-tolyltriethoxysilane 

Downstream Products

• 55577-25-8 2-(4-methylphenyl)-1H-indole 

Relevant academic research and scientific papers

Synthesis method of 2-arylindole derivative

The invention discloses a novel synthesis method of a 2-arylindole derivative. The method comprises the following steps: in an organic solvent, taking an N-(2-pyrimidyl)indole compound and an aryl silane compound as raw materials, taking a catalyst, an oxidizing agent and an activating agent as a catalytic system, carrying out heating and refluxing under stirring, carrying out thin-layer chromatography (TLC) tracking detection until the reaction is complete, and carrying out post-treatment on a reaction solution to obtain the 2-arylindole derivative, wherein the main catalyst is a metal cobaltsalt, the oxidizing agent is copper acetate, and the activating agent is potassium fluoride or cesium fluoride. In the method, cheap metal cobalt is used for catalysis, an oxidative coupling reactionbetween the indole derivative and the aryl silane is realized, and a series of functionalized 2-arylindole compounds are prepared, and the synthesis method of the framework structure is enriched. Simultaneously, the invention provides the novel synthesis method which has low cost, is easy to achieve and is environmentally friendly for synthesis of 2-arylindole compound.

Direct Hiyama Cross-Coupling of (Hetero)arylsilanes with C(sp2)-H Bonds Enabled by Cobalt Catalysis

We report a chelation-assisted C-H arylation of various indoles with sterically and electronically diverse (hetero)arylsilanes enabled by cost-effective Cp*-free cobalt catalysis. Key to the success of this strategy is the judicious choice of copper(II) fluoride as a bifunctional sliane activator and catalyst reoxidant. This methodology features a broad substrate scope and good functional group compatibility. The synthetic versatility of this protocol has been highlighted by the gram-scale synthesis and late-stage diversification of biologically active molecules.

Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C-C bonds

We report here cobalt-N-heterocyclic carbene catalytic systems for the intramolecular decarbonylative coupling through the chelation-assisted C-C bond cleavage of acylindoles and diarylketones. The reaction tolerates a wide range of functional groups such as alkyl, aryl, and heteroaryl groups, giving the decarbonylative products in moderate to excellent yields. This transformation involves the cleavage of two C-C bonds and formation of a new C-C bond without the use of noble metals, thus reinforcing the potential application of decarbonylation as an effective tool for C-C bond formation. This journal is

Nickel-Catalyzed Intramolecular Coupling of Sulfones via the Extrusion of Sulfur Dioxide

We describe a method for intramolecular desulfonylative coupling using bis(cyclooctadiene)nickel as a catalyst. A broad range of aromatic, heteroaromatic and aliphatic sulfones can be utilized as substrates in this process. This method provides an atom-economical route to the synthesis of various biaryls and an efficient tool for the catalytic conversion of sulfonyl groups, representing a significant advancement in organic synthesis. (Figure presented.).

Ruthenium(II)-Catalyzed Direct C-H Arylation of Indoles with Arylsilanes in Water

The ruthenium(II)-catalyzed, heteroatom-directed C-H arylation of indoles with arylsilanes in water has been developed. The method represents the first example of a ruthenium(II)-catalyzed oxidative C-H arylation in water/aqueous media as a sustainable solvent for C-H functionalization. The reaction enables the synthesis of a wide range of indoles with exquisite selectivity for arylation at the C-2 position. Preliminary mechanistic studies indicate reversibility of the C-H ruthenation step under the developed reaction conditions.

Directed Decarbonylation of Unstrained Aryl Ketones via Nickel-Catalyzed C - C Bond Cleavage

The nickel-catalyzed decarbonylation of unstrained diaryl ketones has been developed. The reaction is catalyzed by a combination of Ni(cod)2 and an electron-rich N-heterocyclic carbene ligand. High functional group tolerance and excellent yields (up to 98%) are observed. This strategy provides an alternative and versatile approach to construct biaryls using an inexpensive nickel catalyst.

Suzuki-Miyaura coupling of unstrained ketones via chelation-assisted C-C bond cleavage

Herein, we report that unstrained ketones can be efficiently employed as electrophiles in Suzuki-Miyaura reactions via catalytic activation of unstrained C-C bonds assist by an N-containing directing group. A wide range of aromatic ketones directly coupled with boronic ester with excellent functional group tolerance. This strategy provides an alternative and versatile approach to constructing biaryls from unstrained ketones.

Cobalt(II)-Catalyzed Oxidative C-H Arylation of Indoles and Boronic Acids

Co(II)-catalyzed C-H C2 selective arylation of indoles with boronic acids through monodentate chelation assistance has been achieved for the first time. The unique features of this methodology include mild reaction conditions, highly C2 regioselectivity, and employment of a Grignard reagent-free catalytic system. A wide range of substrates, including unreactive arenes, are well tolerated, which enables the construction of the coupling products efficiently. This new strategy provides an alternative and versatile approach to construct biaryls using inexpensive cobalt catalyst.

Iridium(III)-Catalyzed Direct Arylation of C-H Bonds with Diaryliodonium Salts

By developing a new Ir(III)-catalyzed C-C cross-coupling, a versatile method for direct arylation of sp2 and sp3 C-H bonds in ketoximes, nitrogen-containing heterocycles, various arenes, and olefins has been established. The key to this arylation depends on the appropriate choice of catalyst and the use of diaryliodonium triflate salts as the coupling partners. This transformation has good functional group compatibility and can serve as a powerful synthetic tool for late-stage C-H arylation of complex compounds. Mechanistic studies by density functional theory calculations suggested that the sp3 C-H activation was realized by a triflate-involved concerted metalation-deprotonation process, and the following oxidation of Ir(III) to Ir(V) is the most favorable when a bistriflimide is contained in the diaryliodonium salt. Calculations indicated that both steps are enabled by initial anion exchange between the reactant complexes.

Rhodium-catalyzed regioselective direct C-H arylation of indoles with aryl boronic acids

A highly efficient Rh(III)-catalyzed direct C-H arylation of indoles with aryl boronic acids under mild conditions has been developed. The methodology features wide substrate scope and excellent functional group compatibility (34 examples, up to 99% yield). The arylated products can also be conveniently transformed into biologically active polycyclic indole derivatives.