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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

Hydrosilane-Assisted Synthesis of Urea Derivatives from CO2 and Amines.

TL;DR: A methodology employing CO2, amines, and phenylsilane was discussed to access aryl- or alkyl-substituted urea derivatives, characterized by adopting hydrosilane to promote the formation of ureas directly, without the need to prepare silylamines in advance.
Journal ArticleDOI

Cu nanoparticles: a highly efficient non-noble metal catalyst for rapid reduction of nitro compounds to amines with NaBH4 in water

TL;DR: The purely aqueous phase reduction of a wide range of nitro compounds to the corresponding amines has been carried out with NaBH4 in the presence of inexpensive Cu nanoparticles as catalyst as mentioned in this paper.
Journal ArticleDOI

Synthesis and characterization of magnetically nanoparticles of Fe 3 O 4 @APTMS@ZrCp 2 as a novel and reusable catalyst for convenient reduction of nitro compounds with glycerol

TL;DR: In this paper, the synthesis of magnetically nanoparticles of zirconocene-modified magnetite, Fe3O4@APTMS@ZrCp2, as a new generation in heterogeneous and reusable type nanocatalysts was described.
Journal ArticleDOI

Metal-Free, Rapid, and Highly Chemoselective Reduction of Aromatic Nitro Compounds at Room Temperature.

TL;DR: Under optimal conditions, nitroarenes with sensitive functional groups were converted into the corresponding anilines with excellent selectivity while avoiding the undesirable reduction of thesensitive functional groups.
Journal ArticleDOI

NiCo bimetallic nanoparticles encapsulated in graphite-like carbon layers as efficient and robust hydrogenation catalysts

TL;DR: In this article, the NiCo bimetallic nanoparticles encapsulated in nitrogen doped graphite-like carbon layers (NixCo1−x@NC) with controllable chemical compositions delivered high catalytic performance for hydrogenation of alkenes, alkynes, and nitroarenes.
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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