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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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Porous nanopeapod Pd catalyst with excellent stability and efficiency

TL;DR: Porous Pd@m-C/SiO2 nanopeapods are prepared by a nanoconfinement method showing high efficiency and stability in chemical reactions such as reduction of nitrobenzene by H2 and reduction of NO by NH3.
Journal ArticleDOI

Synthesis of imidazolidin-2-ones employing dialkyl carbonates as an ecofriendly carbonylation source

TL;DR: In this article, a new approach to the synthesis of imidazolidin-2-ones by carbonylation of vicinal diamines with dialkyl carbonates using Pb(NO3)2 and Cu(II) salts as catalysts has been described.
Patent

Aromatic prodrugs of propofol, compositions and uses thereof

Mark A. Gallop, +1 more
TL;DR: Prodrugs of propofol, pharmaceutical compositions of prodrugs, and methods of using prodrug drugs and pharmaceutical compositions to treat or prevent diseases or disorders such as migraine headache pain and post-chemotherapy or post-operative surgery nausea and vomiting are disclosed in this article.
Journal ArticleDOI

Ionic liquid-mediated solvothermal synthesis of 4,4′-methylenediphenyl diisocyanate (MDI): an efficient and environment-friendly process

TL;DR: In this paper, an environment-friendly route is proposed for the synthesis of 4,4′-MDI using 4, 4′-diaminodiphenylmethane and dimethyl carbonate (DMC) as starting materials, which are nontoxic in nature.
Journal ArticleDOI

Application of magnetic Fe3O4 nanoparticles as a reusable heterogeneous catalyst in the synthesis of β-lactams containing amino groups

TL;DR: In this article, the catalytic activity of magnetic Fe3O4 nanoparticles was reported to promote the reduction of β-lactams containing nitroaryl groups to β lactam containing aminoaryl groups in ethanol.
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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