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Dive into the research topics where Apeng Liang is active.

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Featured researches published by Apeng Liang.


Chemical Communications | 2012

The palladium-catalyzed cross-coupling reactions of trifluoroethyl iodide with aryl and heteroaryl boronic acid esters

Apeng Liang; Xinjian Li; Dongfeng Liu; Jingya Li; Dapeng Zou; Yangjie Wu; Yusheng Wu

The cross-coupling reactions of 1,1,1-trifluoro-2-iodoethane with aryl and heteroaryl boronic acid esters have been successfully achieved. The new protocol allows for a convenient introduction of trifluoroethyl groups into a variety of aryl and heteroaryl moieties under mild conditions.


Chemistry: A European Journal | 2016

Regioselective Synthesis of N-Heteroaromatic Trifluoromethoxy Compounds by Direct O-CF3 Bond Formation.

Apeng Liang; Shuaijun Han; Zhenwei Liu; Liang Wang; Jingya Li; Dapeng Zou; Yangjie Wu; Yusheng Wu

The first one-step method for the synthesis of ortho-N-heteroaromatic trifluoromethoxy derivatives by site-specific O-CF3 bond formation using hydroxylated N-heterocycles and Tognis reagent is described. The approach enables the unprecedented syntheses of a wide range of six or five-membered N-heteroaromatic trifluoromethoxy compounds containing one or two heteroatoms from most commonly used hydroxylated N-heterocycles. Notable advantages of this method include its simplicity and mild conditions, avoidance of the need for metals or toxic reagents, and compatibility with a variety of functional groups. Furthermore, this method is especially suitable for the larger scale application.


Journal of Organic Chemistry | 2017

CuI-Catalyzed Fluorodesulfurization for the Synthesis of Monofluoromethyl Aryl Ethers

Yang Geng; Apeng Liang; Xianying Gao; Chengshan Niu; Jingya Li; Dapeng Zou; Yusheng Wu; Yangjie Wu

An efficient CuI-catalyzed fluorodesulfurization for the synthesis of monofluoromethyl aryl ethers using DAST at room temperature has been developed. This approach exhibits a good functional group tolerance, a broad substrate scope, and a high synthesis efficiency.


Organic Letters | 2018

Nickel-Catalyzed Direct C–H Trifluoromethylation of Free Anilines with Togni’s Reagent

Xianying Gao; Yang Geng; Shuaijun Han; Apeng Liang; Jingya Li; Dapeng Zou; Yusheng Wu; Yangjie Wu

An efficient nickel-catalyzed C-H trifluoromethylation for the synthesis of trifluoromethylated free anilines using Tognis reagent has been developed. This approach exhibits a good functional group tolerance, good regioselectivity, and chemoselectivity under mild conditions. The newly developed economical one-step method is a better alternative to synthesize trifluoromethylated free anilines.


Tetrahedron Letters | 2013

Highly efficient synthesis of aryl and heteroaryl trifluoromethyl ketones via o-iodobenzoic acid (IBX)

Huicheng Cheng; Yu Pei; Faqiang Leng; Jingya Li; Apeng Liang; Dapeng Zou; Yangjie Wu; Yusheng Wu


Advanced Synthesis & Catalysis | 2015

Palladium-Catalyzed Carbonylations of Arylboronic Acids: Synthesis of Arylcarboxylic Acid Ethyl Esters

Apeng Liang; Shuaijun Han; Liang Wang; Jingya Li; Dapeng Zou; Yangjie Wu; Yusheng Wu


Tetrahedron Letters | 2017

Copper-Catalyzed Remote C-H Ethoxycarbonyldifluoromethylation of 8-Aminoquinolines with Bis(pinacolato)diboron as Reductant

Shuaijun Han; Apeng Liang; Xiaoxiao Ren; Xianying Gao; Jingya Li; Dapeng Zou; Yangjie Wu; Yusheng Wu


Tetrahedron Letters | 2017

A facile and environmental friendly strategy for the synthesis of N-methoxyquinolin-2(1H)-ones

Xianying Gao; Apeng Liang; Jingya Li; Dapeng Zou; Yangjie Wu; Yusheng Wu


Tetrahedron Letters | 2018

Nickel-catalyzed C H trifluoromethylation of pyridine N -oxides with Togni’s reagent

Xianying Gao; Yang Geng; Shuaijun Han; Apeng Liang; Jingya Li; Dapeng Zou; Yangjie Wu; Yusheng Wu


Tetrahedron Letters | 2014

Synthesis of aryloxyazetidine derivatives by CuI/l-proline catalyzed coupling reaction of arylboronic acid with 1-Boc-3-iodoazetidine

Juanjuan Song; Xinjian Li; Apeng Liang; Jingya Li; Dapeng Zou; Yangjie Wu; Yusheng Wu

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