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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

Hydroamination of isocyanates and isothiocyanates by alkaline earth metal initiators supported by a bulky iminopyrrolyl ligand

TL;DR: A series of new heteroleptic alkaline earth (Ae) metal complexes of general formula [{(Ph2CHNCH)2C4H2N}AeI(THF)3] were synthesized via salt metathesis by reacting potassium salt of ligand 1-K with anhydrous alkaline earth metal diiodides.
Journal ArticleDOI

Synthesis, Structure, and Catalytic Hydrogenation Activity of [NO]-Chelate Half-Sandwich Iridium Complexes with Schiff Base Ligands.

TL;DR: A series of N,O-coordinate iridium(III) complexes with a half-sandwich motif bearing Schiff base ligands for catalytic hydrogenation of nitro and carbonyl substrates have been synthesized.
Journal ArticleDOI

Highly Selective and Efficient Reduction of Nitroarenes by Imidazolium Salt Stabilized Copper Nanoparticles in Aqueous Medium

TL;DR: Imidazolium salt stabilized copper nanoparticles were developed and characterized using TEM, DLS and EDX studies as mentioned in this paper, which greatly enhanced the reactivity and selectivity of reduction reaction in presence of several functional groups in aqueous medium with higher yield.
Journal ArticleDOI

A Facile and Efficient Reduction of Nitroarenes with NiCl2·6H2O/Indium System

TL;DR: In this paper, an efficient and chemoselective method for the reduction of various aromatic nitro compounds to the corresponding amines by treatment with NiCl2·6H2O/In (eq. 1).
Journal ArticleDOI

A Reusable Polymer-anchored Palladium Catalyst for Reduction of Nitroorganics, Alkenes, Alkynes and Schiff Bases†

TL;DR: In this article, the preparation and utility of a new polymer-anchored Pd II catalyst for the hydrogenation of a wide range of organic substrates is described and discussed.
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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