A Convenient Reduction of α,β-Unsaturated Nitroalkenes to Alkylamines Using Boron Hydrides
- 1 October 1984
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 14 (12), 1099-1104
- https://doi.org/10.1080/00397918408059641
Abstract
α,β-Unsaturated nitroalkenes are reduced to alkylamines in good yields by excess of borane-THF in presence of catalytic amount of sodium borohydride.Keywords
This publication has 12 references indexed in Scilit:
- Incorporation of stable and radioactive isotopes via organoborane chemistryAccounts of Chemical Research, 1984
- The Synthesis of Four Possible in vitro Metabolites of the Hallucinogen 1-(2,5-Dimethoxy-4-methylphenyl)-2-aminopropane (DOM)Canadian Journal of Chemistry, 1974
- Analogs of .alpha.-methylphenethylamine (amphetamine). I. Synthesis and pharmacological activity of some methoxy and/or methyl analogsJournal of Medicinal Chemistry, 1970
- Reduction of oximes, oxime ethers, and oxime esters with diborane. Novel synthesis of aminesThe Journal of Organic Chemistry, 1969
- The Six Trimethoxyphenylisopropylamines (Trimethoxyamphetamines)Journal of Medicinal Chemistry, 1966
- Sodium Borohydride Reduction of Nitroso Groups and Furoxan Rings1Journal of the American Chemical Society, 1960
- Reverse Addition of Lithium Aluminum Hydride to NitroölefinsJournal of the American Chemical Society, 1952
- The Reduction of Phenolic β-Nitrostyrenes by Lithium Aluminum HydrideJournal of the American Chemical Society, 1950
- Synthesis of Arylpropylamines. I. From Allyl Chloride1Journal of the American Chemical Society, 1946
- b-PHENYLETHYLAMINEOrganic Syntheses, 1943