THIOL-ACTIVATED SODIUM BOROHYDRIDE REDUCTION OF NITRO COMPOUNDS
- 5 October 1975
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 4 (10) , 1093-1094
- https://doi.org/10.1246/cl.1975.1093
Abstract
Sodium borohydride under the presence of thiols reduced nitro compounds to amine, hydroxylamine, azo, and azoxy compounds.This publication has 5 references indexed in Scilit:
- Reductions with Sulfurated Borohydrides. VI. The Reduction of Nitro, Nitrile, Amide, and Nitroso GroupsCanadian Journal of Chemistry, 1971
- Reduction of aromatic nitro compounds with sodium borohydride in dimethyl sulfoxide or sulfolane. Synthesis of azo or azoxy derivativesThe Journal of Organic Chemistry, 1971
- Chemistry of Sodium Borohydride and Diborane. V. Reduction of Nitrobenzenes with Sodium Borohydride in PyridineCHEMICAL & PHARMACEUTICAL BULLETIN, 1968
- Notes - Hydrogenolysis of 1-Nitronaphthalene by Complex Metal HydridesThe Journal of Organic Chemistry, 1958
- Notes - The Reduction of Nitrobenzene to Azoxybenzene by Sodium BorohydrideThe Journal of Organic Chemistry, 1956