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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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One‐Pot Synthesis of Disubstituted Urea from Carbon Dioxide, Propylene Oxide, and Amines Catalyzed by Imidazolium‐Tetraiodoindate

TL;DR: Guang Meang Son, Cong Chien Truong, Dinesh Kumar Mishra,‡ Vivek Mishra and Yong Jin Kim as mentioned in this paper,§,* † † Department of Chemistry, Yonsei University, Seoul 120-749, Korea ‡ Department of Green Process and System Engineering, Korea University of Science and Technology (UST), Cheonan 31056, Korea Green Material and Process R&D Group, Korea Institute of Industrial Technology (KITECH).
Journal ArticleDOI

Determination and Modeling of Isobaric Vapor–Liquid Equilibria for the Methylcarbamate + Methyl-N-phenyl Carbamate System at Different Pressures

TL;DR: The experimental data were fitted to the Antoine equation with the overall average absolute deviation of pressure of 0.06 kPa and the relative volatility of the binary system was calculated and was more than 1 by far, indicating that high purity MPC can be obtained from the binary mixture by distillation technology as discussed by the authors.
Journal ArticleDOI

RGO/Cu2O-CuO nanocomposite as a visible-light assisted photocatalyst for reduction of organic nitro groups to amines

TL;DR: In this paper, a copper oxide based photocatalyst was developed for the reducing nitrobenzenes to the aminobenzenes using hydrazine monohydrate in the presence of visible light.
Journal ArticleDOI

Samarium‐promoted Chemoselective Reduction of Aromatic Nitro Compounds in Ionic Liquid

TL;DR: The differently substituted aromatic nitro compounds were chemoselectively reduced by Sm/HOAc system in an ionic liquid medium to afford aromatic amines to maintain the other substituents intact.
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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