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Phosphate-modified carbon nanotubes in the oxidative dehydrogenation of isopentanes.
TLDR
It is shown that phosphate can not only impede the total oxidation but also cover the selective C=O groups, hence allowing its use as a modulator to defects and oxygen-containing functional groups on the multiwalled carbon nanotubes, regulating the distribution of active sites and related catalytic targets.
Biological Activities Studies and Phase Transfer Catalysts Promoting the One-Pot Synthesis of N-Aryl-N′-(4-Ethyloxy Benzoyl)-Thiourea Derivatives
A series of N-aryl-N′-(4-ethyloxybenzoyl)-thiourea 3a–h was synthesized under phase transfer catalysis and r.t. conditions. The chemical structure of all compounds were established by IR, 1H NMR, and
One-Pot Synthesis and Crystal Structure of 4-Phenyl-3-[4-chlorophenoloxymethyl]-1H-1,2,4-triazole-5(4H)-thione
4-Phenyl-3-[4-chlorophenoloxymethyl]-1H-1,2,4-triazole-5-thione was synthesized with one-pot method. The structure of the title compound was conformed by IR, 1 H NMR, elemental analysis studies, and
Microwave Promoted Efficient Synthesis of 2,5-Disubstituted 1,3,4-Thiadiazole.
A rapid and efficient method for the synthesis of substituted 1,3,4-thiadiazoles is described. The products have been characterized by analytical and spectral (IR and H'NMR) data.
A Rapid and High-yield Synthesis of Aryloxyacetyl Hydrazides under Microwave Irradiation and with Phase Transfer Catalysis
A series of aryloxyacetyl hydrazides 4a–l were synthesised under microwave irradiation and phase transfer catalysis conditions. By the optimisation of the reaction conditions, a rapid, high-yield and
Rapid and High‐Yield Synthesis of Aryloxyacetates Under Microwave Irradiation and Phase‐Transfer Catalysis Conditions
Abstract A series of methyl aryloxyacetates (3a–3f) have been synthesized by the reaction of substituted phenol with methyl chloroacetate under the conditions of microwave irradiation and
Synthesis and Bioactivity of Some New [3‐[4‐Methylphenoxymethyl]‐4‐phenyl‐[1,2,4]triazole‐5‐thio]acetanilide Derivatives.
The synthesis of some triazole derivatives starting from 4-methyl-phenoloxyacetyl hydrazide is described. In this process, the method for the synthesis of 2-chloroacetanilide had been improved and
5‐(3‐Methyl­phenoxy­meth­yl)‐4‐phenyl‐1,2,4‐triazole‐3‐thione
In the title compound, C16H15N3OS, mol­ecules form inversion-related dimers via N—H⋯S hydrogen bonds. The structure is further stabilized by inter­molecular π–π stacking inter­actions down the a axis.
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