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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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Citations
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Journal ArticleDOI

Highly selective reduction of nitroarenes with gold nano-catalysts immobilized in porous aromatic frameworks

TL;DR: In this paper, the potential coordination sites of phosphine unit and pyridyl group in porous aromatic frameworks (PAFs) were suppressed and AuNPs were evenly dispersed in the resultant Au-PAFs, which exhibited highly efficient and selective catalytic performance for the reduction of nitroarenes.
Journal ArticleDOI

Recent advances in fixation of CO2 into organic carbamates through multicomponent reaction strategies

TL;DR: A review of the recent advances in the synthesis of organic carbamates from CO2 using different multicomponent reaction strategies is presented in this article , where future perspectives and challenges in the incorporation of CO2 into carboxylative cyclization of unsaturated amines are also presented.
Journal ArticleDOI

A study on the heterobinuclear site of Co(salen)/TiO2SiO2 catalysts in the oxidative carbonylation of aniline

TL;DR: Titania-silica immobilized Co(salen) complexes containing the heterobinuclear site were prepared by the sol-gel method for the catalytic synthesis of methyl N-phenylcarbamate (MPC) by the oxidative carbonylation of aniline as mentioned in this paper.
Journal ArticleDOI

Polymer-supported methylselenite for the oxidative carbonylation of aniline

TL;DR: In this paper, the authors showed that poly(1-methyl-3-vinylimidazolium methylselenite) and poly(poly(1ethyl-3vinylenite) can be reused at least up to five times with a moderate loss of activity.
Journal ArticleDOI

A facile reduction of nitroarenes to anilines using FeCl3.6H2O/indium

TL;DR: In this paper, the reduction of a variety of nitroaromatic compounds to corresponding anilines occurs chemoselectively in high yields upon treatment with a new reduction system consisting of FeCl3·6H2O/indium in aqueous methanol.
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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