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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

Transition metal catalyzed hydrogenation or reduction in water

TL;DR: In this article, the authors summarized recent reports on (i) hydrogenation (including transfer hydrogenation by HCO 2 Na) of olefins or aldehydes in water, and (ii) reduction of aromatic compounds with carbon monoxide and water by homogeneous transition metal catalysts.
Journal ArticleDOI

Magnetically recyclable hollow nanocomposite catalysts for heterogeneous reduction of nitroarenes and Suzuki reactions

TL;DR: Highly active magnetically recyclable hollow nanocomposite catalysts with a permeable carbon surface with excellent catalytic activities in the selective reduction of nitroarenes and Suzuki cross-coupling reactions.
Journal ArticleDOI

Away from phosgene: reductive carbonylation of nitroarenes and oxidative carbonylation of amines, understanding the mechanism to improve performance.

TL;DR: Recent progress, with some emphasis on the author's own work, on the understanding of the mechanism of the reductive carbonylation of nitroarenes and of the oxidative carbonylations of amines is discussed, highlighting the close connection between the two reactions.
Journal ArticleDOI

Catalytic activity of mesoporous cobalt oxides with controlled porosity and crystallite sizes: Evaluation using the reduction of 4-nitrophenol

TL;DR: In this article, mesoporous cobalt oxides were synthesized using an inverse surfactant micelle method using mono-dispersed nanoparticle aggregates with connected, well defined intra-particle voids.
Journal ArticleDOI

Reductive Amination without an External Hydrogen Source

TL;DR: A method of reductive amination without an external hydrogen source is reported that proceeds efficiently for a variety of carbonyl compounds and amines at low catalyst loadings and is mechanistically interesting as it does not seem to involve molecular hydrogen.
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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