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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

Improved Method for the Preparation of 1,1-Dimethyl-3-arylureas Using Chlorocarbonylsulfenyl Chloride

TL;DR: In this paper, a procedure for preparing some arylureas having herbicidal properties is reported. But the method has two steps: (1) reaction of arylamine with chlorocarbonylsulfenyl chloride in the presence of nonpolar solvent to produce a ryl carbonyl sulfenyl (CARS) chloride and (2) reaction with dimethylamine in a two-phase reaction catalysed by phase-transfer catalyst to produce the corresponding rryl ureas.
Journal ArticleDOI

Activities of Co(II) Schiff base complexes in the redox carbonylation of aniline and nitrobenzene to methyl N-phenyl carbamate

TL;DR: In this article, a series of cobalt(II) complexes with different Schiff base ligands was synthesized and used as catalyst for the redox carbonylation of aniline and nitrobenzene.
Journal ArticleDOI

Carbonylation of aromatic dinitro compounds with carbon monoxide to respective dicarbamates in the presence of the PdCl2/Fe/I2/Py catalytic system

TL;DR: In this paper, the reductive carbonylation of 1,3dinitrobenzene, 1,4-dinitronzene and 2,4dinitrotoluene to respective dicarbamates in the presence of the PdCl2/Fe/I2/Py catalytic system was investigated.
Book ChapterDOI

Vinyl- and Arylnitrogen Compounds

TL;DR: A review with about 1000 references on new synthetic methods of vinyl and arylnitrogen compounds, covering the period 1995 to ca. mid-2003, can be found in this article.
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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