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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

Demetalation of Silver(III) Corrolates

TL;DR: Electrochemical and chemical reductive methods for silver(III) corrolates demetalation were tested with the aim to avoid the formation of isocorroles and a successful approach was obtained using DBU/THF solutions which afforded the 3-NO(2) corrole free-base compound as a single reaction product in good yield.
Journal ArticleDOI

Room Temperature, Metal-Free Arylation of Aliphatic Alcohols

TL;DR: Diaryliodonium salts are demonstrated as efficient arylating agents of aliphatic alcohols under metal-free conditions and the methodology has been applied to the formal synthesis of butoxycaine.
Journal ArticleDOI

Bonding and Structure of Copper Nitrenes

TL;DR: The ground-state (open-shell) singlet copper nitrene is found to be highly multiconfigurational and to possess a bent geometry about the nitrene nitrogen, contrasting with the linear nitrene geometry of the triplet copper nitrenes.
Journal ArticleDOI

Highly efficient and chemoselective transfer hydrogenation of nitroarenes at room temperature over magnetically separable Fe–Ni bimetallic nanoparticles

TL;DR: In this article, a highly chemoselective catalytic transfer hydrogenation (CTH) of nitroarenes to corresponding amino derivatives is achieved with Fe-Ni bimetallic nanoparticles (FeNi NP's) as the catalyst and NaBH4 at room temperature.
Journal ArticleDOI

Insight into Single-Atom-Induced Unconventional Size Dependence over CeO2-Supported Pt Catalysts

TL;DR: In this paper, an upturned volcanic curve toward the selectivity of p-chloroaniline was found by decreasing the size of Pt from nanoparticles to single atoms, and an unconventional size dependence of Pt toward selective hydrogenation of P-chloronitrobenzene has been extensively investigated over CeO2 support.
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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