Facile hydrogenation of aromatic nuclei with sodium borohydriderhodium chloride in hydroxylic solvents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Reduction of organic compounds with sodium borohydride-transition metal salt systems
2. Reduction of Organic Compounds with NaBH4-Transition Metal Salt Systems. IV. Selective Hydrogenation of Olefines in Unsaturated Esters
3. Reduction of Organic Compounds with Sodium Borohydride-Transition Metal Salt System. III. : Preparation of 2-Aminomethyl-1, 1-diphenyl-1-butene
4. Selective reduction of aromatic nitro compounds with sodium borohydride-stannous chloride.
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1. Sodium Borohydride;Encyclopedia of Reagents for Organic Synthesis;2014-10-20
2. The Binomial Distribution of Hydrogen and Deuterium in Arsanes, Diarsanes, and Triarsanes Generated from As(Iii)/[BHnD4-n]− and the Effect of Trace Amounts of Rh(Iii) Ions;Journal of the American Society for Mass Spectrometry;2012-10-02
3. Sodium Borohydride;Encyclopedia of Reagents for Organic Synthesis;2008-09-15
4. Rhodium(III) Chloride;Encyclopedia of Reagents for Organic Synthesis;2007-09-17
5. Stereocontrolled Access to Orthogonally Protected anti,anti-4-Aminopiperidine-3,5-diols through Chemoselective Reduction of Enantiopure β-Lactam Cyanohydrins;The Journal of Organic Chemistry;2007-09-15
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