Ethyl Acetate as a Pro-Reducing Agent in an One-Pot Reductive Deamination of Nitroanilines

2004 ◽  
Vol 77 (5) ◽  
pp. 1027-1028 ◽  
Author(s):  
Valeriy A. Bacherikov ◽  
May-Jane Wang ◽  
Shu-Yun Cheng ◽  
Ching-Huang Chen ◽  
Kuo-Tung Chen ◽  
...  
Keyword(s):  
Author(s):  
Serap Sahin ◽  
Johan Wärnå ◽  
Päivi Mäki-Arvela ◽  
Tapio Salmi ◽  
Dmitry Yu. Murzin

RSC Advances ◽  
2015 ◽  
Vol 5 (43) ◽  
pp. 33814-33817 ◽  
Author(s):  
Jianhang Huang ◽  
Zhanhong Yang

A ZnO/Ag/polypyrrole (ZAP) composite was synthesized by a facile one-pot method in which silver ammonia complex ions were reduced to metallic silver using a pyrrole monomer as the reducing agent. Meanwhile, the pyrrole monomer was oxidized and formed polypyrrole.


BMC Chemistry ◽  
2020 ◽  
Vol 14 (1) ◽  
Author(s):  
Fereshteh Norouzi ◽  
Shahrzad Javanshir

AbstractA hybrid magnetic material γFe2O3@Sh@cu2O was easily prepared from Shilajit (Sh) decorated Fe3O4 and copper acetate. The prepared magnetic hybrid material was fully characterized using different analysis, including Fourier transform infrared (FT-IR), X-ray diffraction (XRD), inductively coupled plasma (ICP), scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM) thermal gravimetric analysis (TGA) and Brunauer–Emmett–Teller (BET). All these analysis revealed that during coating of Fe3O4@Sh using copper salt (II), synchronized redox sorption of CuII to CuI occurs at the same time as the oxidation of Fe3O4 to γFe2O3. This magnetic catalyst exhibited excellent catalytic activity for regioselective synthesis of 1,4-disubstituted-1,2,3-triazoles via one pot three-component click reaction of sodium azide, terminal alkynes and benzyl halides in the absence of any reducing agent. High yields, short reaction time, high turnover number and frequency (TON = 3.5 * 105 and TOF = 1.0 * 106 h−1 respectively), easy separation, and efficient recycling of the catalyst are the strengths of the present method.


RSC Advances ◽  
2016 ◽  
Vol 6 (100) ◽  
pp. 97629-97635 ◽  
Author(s):  
Hani Nasser Abdelhamid ◽  
Sekar Kumaran ◽  
Hui-Fen Wu

One-pot synthesis of cuprous ferrite (CuFeO2) nanoparticles modified with glycerol (glycerol@CuFeO2 NPs) using oligol and reducing agent was reported.


2015 ◽  
Vol 17 (10) ◽  
Author(s):  
Rashida Parveen ◽  
Janaina F. Gomes ◽  
Sajjad Ullah ◽  
José J. S. Acuña ◽  
Germano Tremiliosi-Filho

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Sidhureddy Boopathi ◽  
Shanmugam Senthilkumar ◽  
Kanala Lakshminarasimha Phani

In this work, we reported for the first time, a facile and one step synthesis of gold nanoparticles from HAuCl4, employing tetraphenylborate as the reducing agent. The synthesis is not only facile but also yields “dumb-bell-shaped”particles. This shape appears to arise from a possible emulsion of the products of oxidation/decomposition of tetraphenylborate by HAuCl4, surrounding the particle. The size and shape of the AuNPs were characterized by Transmission electron microscopy (TEM) and UV-visible Spectroscopy. Interestingly, the addition of polyvinylpyrrolidone (PVP) during the synthesis was found to enhance the stability of the nanoparticle dispersion. The particles synthesized under these conditions assume “spherical” shape with the appearance of only transverse surface plasmon resonance band. The highlight of the observations is that the gold nanoparticles synthesized using tetraphenylborate as reducing agent and PVP as stabilizer are highly stable in alkaline medium, in contrast to the synthesis wherein borohydride is used as reducing agent. The AuNPs synthesized using tetraphenylborate and PVP show their mercury sensing behavior only in the alkaline medium. The color of the nanoparticle dispersion undergoes distinct color change from pink to blue with the addition of mercury ions. They also show dramatic selectivity to mercury ions in presence of other interfering ions, Pb2+, Zn2+and Ca2+.


Author(s):  
DENNIS H. BURNS ◽  
MICHAEL W. BURDEN ◽  
YUE HU LI

A method for the preparation of an α-formylated pyrrole or dipyrromethane which contains an electron-withdrawing β-acetyl is described. Formylation proceeds directly from the corresponding acid pyrrole or dipyrromethane without the need of the usual two-step acid decarboxylation/formylation procedure. The acid is first transformed into its acid chloride with oxalyl chloride, followed by reduction to the aldehyde with the mild reducing agent sodium triacetoxyborohydride, in a one-pot reaction. The non-basic acylating reagent PR 3 is necessary both for acyl chloride formation and for the reduction to succeed.


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