Controlled reduction of nitroalkanes to alkyl hydroxylamines or amines by samarium diiodide
Open Access
- 1 April 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (14) , 1699-1702
- https://doi.org/10.1016/s0040-4039(00)74307-3
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Samarium diiodide - A versatile reagent in organic synthesis.Journal of Synthetic Organic Chemistry, Japan, 1989
- An efficient synthesis of 5-membered cyclic nitrones from γ-nitro ketonesTetrahedron Letters, 1988
- Some Deoxygenation and Reducation Reactions with Samarium DiiodideSynthetic Communications, 1987
- Stereocontrolled cyclization reactions mediated by samarium diiodideJournal of the American Chemical Society, 1987
- Tetrahedron report number 213Tetrahedron, 1986
- Some organic reactions promoted by samarium diiodideJournal of Organometallic Chemistry, 1983
- A Convenient Synthesis of Nitroacetaldehyde DialkylacetalsSynthesis, 1981
- Divalent lanthanide derivatives in organic synthesis. 1. Mild preparation of samarium iodide and ytterbium iodide and their use as reducing or coupling agentsJournal of the American Chemical Society, 1980
- A Preparation of the Ethylene Glycol Mono-Ketal of Cyclohexane-1,4-DioneSynthetic Communications, 1975
- The Reaction of α,β-Unsaturated Aldehydes with Nitro Compounds1,2Journal of the American Chemical Society, 1952