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Journal ArticleDOI

A Review of the Selective Catalytic Reduction of Aromatic Nitro Compounds into Aromatic Amines, Isocyanates, Carbamates, and Ureas Using CO.

Ahmed M. Tafesh, +1 more
- 01 Oct 1996 - 
- Vol. 96, Iss: 6, pp 2035-2052
TLDR
The use of CO as a reductant had been in the past confined to few reactions, but its use in organic synthesis, especially in the reductive carbonylation of nitro aromatics and the oxidative carbonylations of aromatic amines, has increased dramatically as mentioned in this paper.
Abstract
Although the use of CO as a reductant had been in the past confined to few reactions, its use in organic synthesis, especially in the reductive carbonylation of nitro aromatics and the oxidative carbonylation of aromatic amines, has increased dramatically. Since the discovery of CO-induced reduction of nitro groups, there has been a wide spread increase of interest in the application and mechanistic understanding of this reaction. In a major review published in 1988 it was noted, that in practice no studies of the mechanism of N-carbonylation of aromatic nitro compounds with alcohols leading to carbamates have been carried out. This review clearly shows a major change since that publication. Indeed, metal-catalyzed reductive carbonylation of nitro aromatics using CO as reducing agent has been in the past 10 years the subject of intense investigation both in academia and in the chemical industry. Several articles and reviews have covered the subject up to the late 1980s. The authors will concentrate on more recent literature, but sometimes older data will be used to establish an understanding of these reactions. 127 refs.

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Journal ArticleDOI

Two-step one-pot electrosynthesis and catalytic activity of xCoO–yCo(OH) 2 -supported silver nanoparticles

TL;DR: In this paper, an efficient two-step electrosynthesis of xCoO-yCo(OH)2 (CoOxHy)-supported silver nanoparticles (AgNPs) is carried out in N,N-dimethylformamide (DMF) using atmospheric oxygen as a reagent and mediator at the potentials of its reduction to the superoxide ion.
Journal ArticleDOI

Highly dispersed Ru anchored on nanosheet N-doped carbon for efficient and chemoselective hydrogenation of nitroaromatics to aromatic amines under mild conditions

TL;DR: In this article , a series of N-doped carbon (NC-x) with high nitrogen contents were firstly synthesized by pyrolysis of 1-butyl-3-vinylimidazolium bromide-co-acrylonitrile with a template of g-C 3 N 4 .
Journal ArticleDOI

Highly dispersed Ru anchored on nanosheet N-doped carbon for efficient and chemoselective hydrogenation of nitroaromatics to aromatic amines under mild conditions

TL;DR: In this article, a series of N-doped carbon (NC-x) with high nitrogen contents were firstly synthesized by pyrolysis of 1-butyl-3-vinylimidazolium bromide-co-acrylonitrile with a template of g-C3N4.
Journal ArticleDOI

Cobalt Complexes Catalyze Reduction of Nitro Compounds: Mechanistic Studies

TL;DR: Mononuclear Co2+/3+ complexes of 13-membered amide-based macrocycles have been synthesized, characterized and utilized in the chemo-selective reduction of assorted nitro compounds including aromatic, heterocyclic and aliphatic ones as mentioned in this paper.
References
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Journal ArticleDOI

Water-Soluble Ligands, Metal Complexes, and Catalysts: Synergism of Homogeneous and Heterogeneous Catalysis

TL;DR: Water-soluble catalysts as mentioned in this paper combine the advantages of homogeneous and heterogeneous catalysis: simple and complete separation of the product from the catalyst, high activity, and high selectivity.
Journal ArticleDOI

Palladium(II) catalysts for living alternating copolymerization of olefins and carbon monoxide

TL;DR: In this article, the synthesis of well-defined Pd(II) catalysts that operate in aprotic solvents to yield living alternating copolymers of olefins and CO was reported.
Journal ArticleDOI

Palladium Complex-Catalyzed Reductive N-Heterocyclization of Nitroarenes: Novel Synthesis of Indole and 2H-Indazole Derivatives

TL;DR: The dichlorobis(triphenylphosphine)palladium (PdCl 2 (PPh 3 ) 1 )-tin(II) chloride (SnCl 2 ) system showed high catalytic activity for the reductive N-heterocyclization of various 2-nitrostyrene and N-(2-nitrobenzylidene)amine derivatives when employed at 100 o C for 16 h under 20 kg cm -2 of initial carbon monoxide pressure, to give the corresponding indole and 2H-indazole derivatives in
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