ChemInform Abstract: STUDIES ON AROMATIC NITRO COMPOUNDS. V. A SIMPLE ONE-POT PREPARATION OF O-AMINOAROYLNITRILES FROM SOME AROMATIC NITRO COMPOUNDS

1985 ◽  
Vol 16 (36) ◽  
Author(s):  
Y. TOMIOKA ◽  
K. OHKUBO ◽  
M. YAMAZAKI
Keyword(s):  
Nitro Compounds ◽  
One Pot ◽  
Aromatic Nitro Compounds ◽  
Aromatic Nitro

One-pot synthesis of Ni–NiFe2O4/carbon nanofiber composites from biomass for selective hydrogenation of aromatic nitro compounds

2015 ◽  
Vol 17 (2) ◽  
pp. 821-826 ◽  
Author(s):  
Wu-Jun Liu ◽  
Ke Tian ◽  
Hong Jiang
Keyword(s):  
Catalytic Hydrogenation ◽  
Selective Hydrogenation ◽  
Carbon Nanofiber ◽  
Fast Pyrolysis ◽  
Nitro Compounds ◽  
One Pot ◽  
Aromatic Nitro Compounds ◽  
One Pot Synthesis ◽  
Aromatic Nitro

Ni–NiFe2O4/carbon nanofiber composites with a favourable performance in catalytic hydrogenation were synthesized by fast pyrolysis of FeCl3 and NiCl2 preloaded biomass.

scholarly journals Immobilized antimony species on magnetite: a novel and highly efficient magnetically reusable nanocatalyst for direct and gram-scale reductive-coupling of nitroarenes to azoarenes

RSC Advances ◽  
2019 ◽  
Vol 9 (23) ◽  
pp. 13112-13121 ◽  
Author(s):  
Behzad Zeynizadeh ◽  
Fariba Faraji
Keyword(s):  
Catalytic Activity ◽  
Magnetic Nanoparticles ◽  
Nitro Compounds ◽  
Reductive Coupling ◽  
One Pot ◽  
Highly Efficient ◽  
Aromatic Nitro Compounds ◽  
Aromatic Nitro

In this study, magnetic nanoparticles of Fe3O4@SbFx were synthesized. Then, the catalytic activity of Fe3O4@SbFx MNPs was highlighted by one-pot reductive-coupling of aromatic nitro compounds to the corresponding azoarene materials with NaBH4.

Unexpected reactivity between aromatic nitro compounds and PCl3/AlCl3. A new one-pot synthesis of phenazines

2003 ◽  
Vol 44 (13) ◽  
pp. 2649-2653 ◽  
Author(s):  
Rodolphe Abdayem ◽  
Graziano Baccolini ◽  
Carla Boga ◽  
Magda Monari ◽  
Simona Selva
Keyword(s):  
Nitro Compounds ◽  
One Pot ◽  
Aromatic Nitro Compounds ◽  
One Pot Synthesis ◽  
Aromatic Nitro

A One-Pot Approach to 2-(N-Substituted Amino)-1,4-naphthoquinones with Use of Nitro Compounds and 1,4-Naphthoquinones in Water

Synlett ◽  
2019 ◽  
Vol 30 (05) ◽  
pp. 615-619 ◽  
Author(s):  
Ji-Yu Wang ◽  
Xu-Ling Chen ◽  
Yu Dong ◽  
Shuai He ◽  
Rui Zhang ◽  
...  
Keyword(s):  
Functional Groups ◽  
Nitro Compounds ◽  
Reaction Conditions ◽  
One Pot ◽  
Aliphatic Nitro Compounds ◽  
Aromatic Nitro Compounds ◽  
One Pot Synthesis ◽  
Aromatic Nitro

A one-pot synthesis of 2-(N-substituted amino)-1,4-naphthoquinones from 1,4-naphthoquinones and nitro compounds in water has been developed. This method features mild reaction conditions and provides aromatic nitro compounds with various functional groups such as halogens, methylthio, ester, amide, even allyl, propargyl, and heterocycles, as well as aliphatic nitro compounds that are well tolerated. This method can be scaled up and we conducted further transformation of the obtained 2-(N-substituted amino)-1,4-naphthoquinones to synthesize carbazolequinone derivatives.

scholarly journals Two different facile and efficient approaches for the synthesis of various N-arylacetamides via N-acetylation of arylamines and straightforward one-pot reductive acetylation of nitroarenes promoted by recyclable CuFe2O4 nanoparticles in water

2019 ◽  
Vol 8 (1) ◽  
pp. 742-755 ◽  
Author(s):  
Behzad Zeynizadeh ◽  
Farkhondeh Mohammad Aminzadeh ◽  
Hossein Mousavi
Keyword(s):  
Magnetic Field ◽  
External Magnetic Field ◽  
Nitro Compounds ◽  
Significant Loss ◽  
Environmentally Benign ◽  
One Pot ◽  
Aromatic Nitro Compounds ◽  
Aromatic Nitro

Abstract Two simple, efficient, and environmentally benign protocols for the synthesis of various N-arylacetamides via N-acetylation of arylamines and straightforward one-pot reductive acetylation of aromatic nitro compounds promoted by CuFe2O4 nanoparticles in water at reflux have been developed. The prepared CuFe2O4 MNPs are well known and fully characterized by various techniques. Furthermore, the CuFe2O4 NPs easily separated from the reaction environment using an external magnetic field and can be reused for several times without significant loss of its activity for both mentioned reactions.

scholarly journals One-pot efficient reductive acetylation of aromatic nitro compounds

2014 ◽  
Vol 7 (4) ◽  
pp. 30-40 ◽  
Author(s):  
Kaushik Basu ◽  
◽  
Suchandra Chakraborty ◽  
Chandan Saha ◽  
Achintya Kumar Sarkar
Keyword(s):  
Nitro Compounds ◽  
One Pot ◽  
Aromatic Nitro Compounds ◽  
Aromatic Nitro
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