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Active nickel-based reduction of organic compounds
Authors:Alonso  F  Radivoy  G  Yus  M
Institution:(1) Department of Organic Chemistry, Faculty of Sciences, Alicante University, Apdo. 99, E-03080 Alicante, Spain;(2) Department of Chemistry, Institute of Research in Organic Chemistry (INIQO), National Southern University, 1253 Alem, 8000 Bahía Blanca, Argentina
Abstract:The reducing system NiCl2·2H2O—Li—arenecat (cat is catalyst) was proposed for use to reduce a wide range of organic compounds, including alkenes, alkynes, carbonyl compounds, imines, halogenated derivatives, sulfonates, aromatic compounds, hydrazines, azo and azoxy compounds, N-oxides, and nitrones. The degree of reduction can be controlled for some substrates. Deuterium can be incorporated in the reaction products using nickel chloride deuteriohydrate. Nitrones, N-alkoxyamides, and acyl azides are also reduced with the Li—arenecat system containing no nickel salt.
Keywords:organic compounds  reduction  active metals  catalysis by arenes
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