Relevant bibliographies by topics / Nitro groups reduction

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  1. Journal articles

Academic literature on the topic 'Nitro groups reduction'

Author: Grafiati
Published: 9 March 2023

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Journal articles on the topic "Nitro groups reduction"

1

Khan, Rahat H. "Tellurium mediated reduction of aromatic nitro groups." Journal of Chemical Research 2000, no. 6 (2000): 290–91. http://dx.doi.org/10.3184/030823400103167336.

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2

Riley, Darren, and Nicole Neyt. "Approaches for Performing Reductions under Continuous-Flow Conditions." Synthesis 50, no. 14 (2018): 2707–20. http://dx.doi.org/10.1055/s-0037-1610153.

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A concise overview of approaches to perform reductions of various functionalities including aldehydes, ketones, esters, imines, ­nitriles, nitro groups, alkenes and alkynes under continuous-flow conditions are highlighted and discussed in this short review.1 Introduction2 Reduction of Aldehydes, Ketones and Esters3 Reduction of Imines and Nitriles4 Reduction of Nitro Groups5 Reduction of Alkenes6 Partial Reduction of Alkynes7 Conclusion
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3

Khan, Rahat H. "ChemInform Abstract: Tellurium Mediated Reduction of Aromatic Nitro Groups." ChemInform 31, no. 44 (2000): no. http://dx.doi.org/10.1002/chin.200044049.

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4

G.O., Obaiah, Shivaprasad K.H., Shrikanth K. Bhat, and Mylarappa M. "Selective Reduction of Aromatic Nitro Compounds to Amines From Pd Doped TiO2 Catalyzed Nano Catalyst." ECS Transactions 107, no. 1 (2022): 1681–87. http://dx.doi.org/10.1149/10701.1681ecst.

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An efficient chemoselective reduction of aromatic nitro compounds to corresponding amino analogs was achieved using palladium doped TiO2 (Ti0.97Pd0.03O1.97) nanoparticles. The reductions are effectively carried out in the presence of aromatic nitro compounds of various other reducible functional groups such as halo, alkoxy, carbonyl, and cyanide. The reduction of aromatic nitro compounds to aromatic amines was recognized with excellent yield (100%) by using nano porous palladium as a sustainable catalyst and as a hydrogen source. Reduced amines were well characterized using PXRD, 1H NMR, and 1
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5

Moody, Christopher J., and Michael R. Pitts. "Indium as a Reducing Agent: Reduction of Aromatic Nitro Groups." Synlett 1998, no. 9 (1998): 1028. http://dx.doi.org/10.1055/s-1998-1837.

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6

Huber, Didier, Guy Andermann, and Gérard Leclerc. "Selective reduction of aromatic / aliphatic nitro groups by sodium sulfide." Tetrahedron Letters 29, no. 6 (1988): 635–38. http://dx.doi.org/10.1016/s0040-4039(00)80169-0.

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7

Austin, Rupert P., and John H. Ridd. "Novel oxidation reduction reactions involving nitro groups and methyl groups in trifluoromethanesulfonic acid." Journal of the Chemical Society, Chemical Communications, no. 21 (1992): 1599. http://dx.doi.org/10.1039/c39920001599.

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8

Dood, Amber, Patrick Fisher, Christine Bodden, et al. "Synthesis of 5,6-Diaminoacenaphthylene by Reduction of Sterically Crowded Nitro Groups with Sodium Dithionite." SynOpen 02, no. 04 (2018): 0312–15. http://dx.doi.org/10.1055/s-0037-1610406.

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5,6-Diaminoacenaphthylene was synthesized in four steps from acenaphthene. This seemingly simple molecule provides unique synthetic challenges because it is relatively difficult to reduce the nitro groups and the molecule contains a particularly reactive double bond. It was determined that the only feasible sequence for the synthesis was to nitrate acenaphthene, then brominate, eliminate, and finally selectively reduce. Several reduction methods were attempted before finding one that would completely reduce both nitro groups while leaving the double bond intact.
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9

AUSTIN, R. P., and J. H. RIDD. "ChemInform Abstract: Novel Oxidation Reduction Reactions Involving Nitro Groups and Methyl Groups in Trifluoromethanesulfonic Acid." ChemInform 24, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199306129.

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10

Sun, Shuai, Zhengjun Quan, and Xicun Wang. "Selective reduction of nitro-compounds to primary amines by nickel-catalyzed hydrosilylative reduction." RSC Advances 5, no. 103 (2015): 84574–77. http://dx.doi.org/10.1039/c5ra17731f.

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The tolerances of many functional groups, e.g. aryl-chloride, aryl-bromide, alkene, alkynyl, ester, ether, oxhydryl, carboxylic acid, cyano group, nitrine, carbonyl, acyl, thioether and some heterocycles, were studied with unprecedentedly high chemoselectivity.
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