scholarly journals Integrated Experimental and Theoretical Study of Shape-Controlled Catalytic Oxidative Coupling of Aromatic Amines over CuO Nanostructures

ACS Omega ◽  
2016 ◽  
Vol 1 (6) ◽  
pp. 1121-1138 ◽  
Author(s):  
Ramana Singuru ◽  
Quang Thang Trinh ◽  
Biplab Banerjee ◽  
Bolla Govinda Rao ◽  
Linyi Bai ◽  
...  
Keyword(s):  
Oxidative Coupling ◽  
Aromatic Amines ◽  
Theoretical Study ◽  
Shape Controlled

Interface Engineering of Graphene-Supported Cu Nanoparticles Encapsulated by Mesoporous Silica for Size-Dependent Catalytic Oxidative Coupling of Aromatic Amines

2019 ◽  
Vol 11 (12) ◽  
pp. 11722-11735 ◽  
Author(s):  
Chitra Sarkar ◽  
Saikiran Pendem ◽  
Abhijit Shrotri ◽  
Duy Quang Dao ◽  
Phuong Pham Thi Mai ◽  
...  
Keyword(s):  
Mesoporous Silica ◽  
Oxidative Coupling ◽  
Aromatic Amines ◽  
Cu Nanoparticles ◽  
Interface Engineering ◽  
Size Dependent

A theoretical study of the carcinogenic nature of some aromatic amines

1980 ◽  
Vol 86 (3) ◽  
pp. 577-580 ◽  
Author(s):  
R.A. Thuraisingham ◽  
S.H.M Nilar
Keyword(s):  
Aromatic Amines ◽  
Theoretical Study

ChemInform Abstract: Oxidative Coupling of 1,5-Dihydroxynaphthalene with Aromatic Amines.

ChemInform ◽  
2010 ◽  
Vol 23 (29) ◽  
pp. no-no
Author(s):  
L. V. EKTOVA ◽  
R. P. SHISHKINA
Keyword(s):  
Oxidative Coupling ◽  
Aromatic Amines

Theoretical study of the oxidation mechanism of aromatic amines

1991 ◽  
pp. 1437-1443 ◽  
Author(s):  
Daniel Larumbe ◽  
Miquel Moreno ◽  
Iluminada Gallardo ◽  
Juan Bertrán ◽  
Claude P. Andrieux
Keyword(s):  
Aromatic Amines ◽  
Theoretical Study ◽  
Oxidation Mechanism

scholarly journals On-Water Reactivity and Regioselectivity of Quinones in C–N Coupling with Amines: Experimental and Theoretical Study

2014 ◽  
Vol 67 (2) ◽  
pp. 217 ◽  
Author(s):  
Maximiliano Martínez-Cifuentes ◽  
Graciela Clavijo-Allancan ◽  
Carolina Di Vaggio-Conejeros ◽  
Boris Weiss-López ◽  
Ramiro Araya-Maturana
Keyword(s):  
Density Functional Theory ◽  
Oxidative Coupling ◽  
Density Functional ◽  
Molecular Electrostatic Potential ◽  
Theoretical Study ◽  
Chemical Reactivity ◽  
Organic Medium ◽  
Conceptual Density Functional Theory ◽  
Functional Theory ◽  
Water Conditions

A study about the oxidative coupling of some representative carbo- and heterocyclic non-symmetrical quinones with aryl- and alkylamines, was carried out comparing dichloromethane and water as reaction mediums. We found that the on-water reactions gave better or, at worst, the same results as a conventional organic medium like dichloromethane. Descriptors derived from conceptual density functional theory and approaches of electrostatic nature, such as the molecular electrostatic potential, were used to explain the observed chemical reactivity and regioselectivity. Further, the on-water conditions were used to obtain 24 new aminoquinones with potential biological activity.

Towards the rational biosynthesis of substituted phenazines and phenoxazinones by laccases

2014 ◽  
Vol 16 (9) ◽  
pp. 4127-4136 ◽  
Author(s):  
Ana Catarina Sousa ◽  
M. Conceição Oliveira ◽  
Lígia O. Martins ◽  
M. Paula Robalo
Keyword(s):  
Oxidative Coupling ◽  
Aromatic Amines

The laccase-catalysed oxidative coupling of substituted aromatic amines is described, extending the scope of laccases towards the production of phenazine and phenoxazinone derivatives.

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